2021
van der Wee, Ernest B; Fokkema, Jantina; Kennedy, Chris L; Pozo, Marc Del; de Winter, D A Matthijs; Speets, Peter N A; Gerritsen, Hans C; van Blaaderen, Alfons
3D test sample for the calibration and quality control of stimulated emission depletion (STED) and confocal microscopes Journal Article
In: Commun Biol, vol. 4, no. 1, pp. 909, 2021, ISSN: 2399-3642.
@article{pmid34302049,
title = {3D test sample for the calibration and quality control of stimulated emission depletion (STED) and confocal microscopes},
author = {Ernest B van der Wee and Jantina Fokkema and Chris L Kennedy and Marc Del Pozo and D A Matthijs de Winter and Peter N A Speets and Hans C Gerritsen and Alfons van Blaaderen},
doi = {10.1038/s42003-021-02432-3},
issn = {2399-3642},
year = {2021},
date = {2021-01-01},
urldate = {2021-01-01},
journal = {Commun Biol},
volume = {4},
number = {1},
pages = {909},
abstract = {Multiple samples are required to monitor and optimize the quality and reliability of quantitative measurements of stimulated emission depletion (STED) and confocal microscopes. Here, we present a single sample to calibrate these microscopes, align their laser beams and measure their point spread function (PSF) in 3D. The sample is composed of a refractive index matched colloidal crystal of silica beads with fluorescent and gold cores. The microscopes can be calibrated in three dimensions using the periodicity of the crystal; the alignment of the laser beams can be checked using the reflection of the gold cores; and the PSF can be measured at multiple positions and depths using the fluorescent cores. It is demonstrated how this sample can be used to visualize and improve the quality of STED and confocal microscopy images. The sample is adjustable to meet the requirements of different NA objectives and microscopy techniques and additionally can be used to evaluate refractive index mismatches as a function of depth quantitatively.},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
Aslannejad, H.; Loginov, Sergey V.; Hoek, B.; Schoonderwoerd, E. M.; Gerritsen, Hans C; Hassanizadeh, S. M.
Liquid droplet imbibition into a thin coating layer: Direct pore-scale modeling and experimental observations Journal Article
In: Progress in Organic Coatings, vol. 151, pp. 106054, 2021, ISSN: 0300-9440.
@article{ASLANNEJAD2021106054,
title = {Liquid droplet imbibition into a thin coating layer: Direct pore-scale modeling and experimental observations},
author = {H. Aslannejad and Sergey V. Loginov and B. Hoek and E. M. Schoonderwoerd and Hans C Gerritsen and S. M. Hassanizadeh},
url = {https://www.sciencedirect.com/science/article/pii/S0300944020312650},
doi = {https://doi.org/10.1016/j.porgcoat.2020.106054},
issn = {0300-9440},
year = {2021},
date = {2021-01-01},
journal = {Progress in Organic Coatings},
volume = {151},
pages = {106054},
abstract = {In order to control ink droplet movement into the printing-paper layer, a set of pore-scale two-phase flow simulations were performed. The high-resolution three-dimensional pore space of the paper was obtained using focused ion beam scanning electron microscopy (FIB-SEM). Solving Navier-Stokes equations yielded details about dynamic movement of a droplet into the layer. To evaluate simulation results, for the first time, confocal laser microscopy imaging technique was integrated into a FIB-SEM chamber. Doing so, high resolution imaging of the droplet penetration inside paper was conducted and computed volume of penetrated ink at final stage was compared to the imaged volume. The ink penetration and spreading extent showed a good agreement with simulation results. Therefore, the developed simulation case was further investigated to study impact of liquid contact angle, real ink properties, and droplet arrival velocity on paper surface on final print quality. A faster penetration into the paper coating was observed for smaller equilibrium contact angles; meanwhile, more radial wicking was observed. In case of velocity of impact, higher velocity caused creation of irregular shapes of the ink footprint on paper surface. In addition to that, higher velocity caused ink splash which consequently created satellite droplets and lowered the print quality. Comparing ink-like liquid (representing real ink liquid properties) with water, water moves faster than ink-like liquid into the paper. This is mainly due to the higher viscosity and lower surface tension of the ink-like liquid.},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
Xia, Chenghui; Pedrazo-Tardajos, Adrian; Wang, Da; Meeldijk, Johannes D.; Gerritsen, Hans C.; Bals, Sara; Donega, Celso Mello
Seeded Growth Combined with Cation Exchange for the Synthesis of Anisotropic Cu2–xS/ZnS, Cu2–xS, and CuInS2 Nanorods Journal Article
In: Chemistry of Materials, vol. 33, no. 1, pp. 102-116, 2021, (PMID: 33456135).
@article{doi:10.1021/acs.chemmater.0c02817,
title = {Seeded Growth Combined with Cation Exchange for the Synthesis of Anisotropic Cu2–xS/ZnS, Cu2–xS, and CuInS2 Nanorods},
author = {Chenghui Xia and Adrian Pedrazo-Tardajos and Da Wang and Johannes D. Meeldijk and Hans C. Gerritsen and Sara Bals and Celso Mello Donega},
url = {https://doi.org/10.1021/acs.chemmater.0c02817},
doi = {10.1021/acs.chemmater.0c02817},
year = {2021},
date = {2021-01-01},
journal = {Chemistry of Materials},
volume = {33},
number = {1},
pages = {102-116},
abstract = {Colloidal copper(I) sulfide (Cu2–xS) nanocrystals (NCs) have attracted much attention for a wide range of applications because of their unique optoelectronic properties, driving scientists to explore the potential of using Cu2–xS NCs as seeds in the synthesis of heteronanocrystals to achieve new multifunctional materials. Herein, we developed a multistep synthesis strategy toward Cu2–xS/ZnS heteronanorods. The Janus-type Cu2–xS/ZnS heteronanorods are obtained by the injection of hexagonal high-chalcocite Cu2–xS seed NCs in a hot zinc oleate solution in the presence of suitable surfactants, 20 s after the injection of sulfur precursors. The Cu2–xS seed NCs undergo rapid aggregation and coalescence in the first few seconds after the injection, forming larger NCs that act as the effective seeds for heteronucleation and growth of ZnS. The ZnS heteronucleation occurs on a single (100) facet of the Cu2–xS seed NCs and is followed by fast anisotropic growth along a direction that is perpendicular to the c-axis, thus leading to Cu2–xS/ZnS Janus-type heteronanorods with a sharp heterointerface. Interestingly, the high-chalcocite crystal structure of the injected Cu2–xS seed NCs is preserved in the Cu2–xS segments of the heteronanorods because of the high-thermodynamic stability of this Cu2–xS phase. The Cu2–xS/ZnS heteronanorods are subsequently converted into single-component Cu2–xS and CuInS2 nanorods by postsynthetic topotactic cation exchange. This work expands the possibilities for the rational synthesis of colloidal multicomponent heteronanorods by allowing the design principles of postsynthetic heteroepitaxial seeded growth and nanoscale cation exchange to be combined, yielding access to a plethora of multicomponent heteronanorods with diameters in the quantum confinement regime.},
note = {PMID: 33456135},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
Buerger, Korbinian; Schmidt, Kerstin N.; Fokkema, Jantina; Gerritsen, Hans C.; Maier, Olga; Vries, Uwe; Zaytseva, Yulia; Rachel, Reinhard; Witzgall, Ralph
Chapter 8 - On-section correlative light and electron microscopy of large cellular volumes using STEM tomography Incollection
In: Müller-Reichert, Thomas; Verkade, Paul (Ed.): Correlative Light and Electron Microscopy IV, vol. 162, pp. 171-203, Academic Press, 2021, ISSN: 0091-679X.
@incollection{BUERGER2021171,
title = {Chapter 8 - On-section correlative light and electron microscopy of large cellular volumes using STEM tomography},
author = {Korbinian Buerger and Kerstin N. Schmidt and Jantina Fokkema and Hans C. Gerritsen and Olga Maier and Uwe Vries and Yulia Zaytseva and Reinhard Rachel and Ralph Witzgall},
editor = {Thomas Müller-Reichert and Paul Verkade},
url = {https://www.sciencedirect.com/science/article/pii/S0091679X2030176X},
doi = {https://doi.org/10.1016/bs.mcb.2020.09.002},
issn = {0091-679X},
year = {2021},
date = {2021-01-01},
booktitle = {Correlative Light and Electron Microscopy IV},
volume = {162},
pages = {171-203},
publisher = {Academic Press},
series = {Methods in Cell Biology},
abstract = {The application of both fluorescence and electron microscopy results in a powerful combination of imaging modalities called “correlative light and electron microscopy” (CLEM). Whereas conventional transmission electron microscopy (TEM) tomography is only able to image sections up to a thickness of ~300nm, scanning transmission electron microscopy (STEM) tomography at 200kV allows the analysis of sections up to a thickness of 900nm in three dimensions. In the current study we have successfully integrated STEM tomography into CLEM as demonstrated for human retinal pigment epithelial 1 (RPE1) cells expressing various fluorescent fusion proteins which were high-pressure frozen and then embedded in Lowicryl HM20. Fluorescently labeled gold nanoparticles were applied onto resin sections and imaged by fluorescence and electron microscopy. STEM tomograms were recorded at regions of interest, and overlays were generated using the eC-CLEM software package. Through the nuclear staining of living cells, the use of fluorescently labeled gold fiducials for the generation of overlays, and the integration of STEM tomography we have markedly extended the application of the Kukulski protocol (Kukulski et al., 2011, 2012). Various fluorescently tagged proteins localizing to different cellular organelles could be assigned to their ultrastructural compartments. By combining STEM tomography with on-section CLEM, fluorescently tagged proteins can be localized in three-dimensional ultrastructural environments with a volume of at least 2.7×2.7×0.5μm.},
keywords = {},
pubstate = {published},
tppubtype = {incollection}
}
2020
Lehmann, K; Shayegan, M; Blab, Gerhard A.; Forde, N R
Optical Tweezers Approaches for Probing Multiscale Protein Mechanics and Assembly Journal Article
In: Frontiers in Molecular Biosciences, vol. 7, 2020.
@article{lehmann_optical_2020,
title = {Optical Tweezers Approaches for Probing Multiscale Protein Mechanics and Assembly},
author = {K Lehmann and M Shayegan and Gerhard A. Blab and N R Forde},
url = {https://www.frontiersin.org/articles/10.3389/fmolb.2020.577314/full},
doi = {10.3389/fmolb.2020.577314},
year = {2020},
date = {2020-01-01},
urldate = {2020-01-01},
journal = {Frontiers in Molecular Biosciences},
volume = {7},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
Mohammadian, Sajjad; Agronskaia, Alexandra V; Blab, Gerhard A.; van Donselaar, E G; de Heus, C; Liv, N; Klumperman, J; Gerritsen, Hans C.
Integrated super resolution fluorescence microscopy and transmission electron microscopy Journal Article
In: Ultramicroscopy, vol. 215, 2020.
@article{mohammadian_integrated_2020,
title = {Integrated super resolution fluorescence microscopy and transmission electron microscopy},
author = {Sajjad Mohammadian and Alexandra V Agronskaia and Gerhard A. Blab and E G van Donselaar and C de Heus and N Liv and J Klumperman and Hans C. Gerritsen},
url = {https://www.scopus.com/inward/record.uri?eid=2-s2.0-85085254573&doi=10.1016%2fj.ultramic.2020.113007&partnerID=40&md5=d0486d73138b228cf6091bd2e59de054},
doi = {10.1016/j.ultramic.2020.113007},
year = {2020},
date = {2020-01-01},
journal = {Ultramicroscopy},
volume = {215},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
Soeteman-Hernández, L G; Blab, Gerhard A.; Carattino, A; Dekker, F; Dekkers, S; van der Linden, M; van Silfhout, A; Noorlander, C W
Challenges of implementing nano-specific safety and safe-by-design principles in academia Journal Article
In: NanoImpact, vol. 19, 2020.
@article{soeteman-hernandez_challenges_2020,
title = {Challenges of implementing nano-specific safety and safe-by-design principles in academia},
author = {L G Soeteman-Hernández and Gerhard A. Blab and A Carattino and F Dekker and S Dekkers and M van der Linden and A van Silfhout and C W Noorlander},
url = {https://www.scopus.com/inward/record.uri?eid=2-s2.0-85089135360&doi=10.1016%2fj.impact.2020.100243&partnerID=40&md5=95e711c68da63f49c51e21c9a9b22648},
doi = {10.1016/j.impact.2020.100243},
year = {2020},
date = {2020-01-01},
journal = {NanoImpact},
volume = {19},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
2019
van Hest, Jacobine J. H. A.; Agronskaia, Alexandra V.; Fokkema, Jantina; Montanarella, F.; Puig, A. Gregorio; de Mello Donega, Celso; Meijerink, Andries; Blab, Gerhard A.; Gerritsen, Hans C.
Towards robust and versatile single nanoparticle fiducial markers for correlative light and electron microscopy Journal Article
In: Journal of Microscopy, vol. 274, no. 1, pp. 13–22, 2019.
@article{van_hest_towards_2019,
title = {Towards robust and versatile single nanoparticle fiducial markers for correlative light and electron microscopy},
author = { Jacobine J.H.A. van Hest and Alexandra V. Agronskaia and Jantina Fokkema and F. Montanarella and A. Gregorio Puig and Celso de Mello Donega and Andries Meijerink and Gerhard A. Blab and Hans C. Gerritsen},
doi = {10.1111/jmi.12778},
year = {2019},
date = {2019-01-01},
journal = {Journal of Microscopy},
volume = {274},
number = {1},
pages = {13--22},
abstract = {Fiducial markers are used in correlated light and electron microscopy (CLEM) to enable accurate overlaying of fluorescence and electron microscopy images. Currently used fiducial markers, e.g. dye-labelled nanoparticles and quantum dots, suffer from irreversible quenching of the luminescence after electron beam exposure. This limits their use in CLEM, since samples have to be studied with light microscopy before the sample can be studied with electron microscopy. Robust fiducial markers, i.e. luminescent labels that can (partially) withstand electron bombardment, are interesting because of the recent development of integrated CLEM microscopes. In addition, nonintegrated CLEM setups may benefit from such fiducial markers. Such markers would allow switching back from EM to LM and are not available yet. Here, we investigate the robustness of various luminescent nanoparticles (NPs) that have good contrast in electron microscopy; 130 nm gold-core rhodamine B-labelled silica particles, 15 nm CdSe/CdS/ZnS core–shell–shell quantum dots (QDs) and 230 nm Y 2 O 3 :Eu 3+ particles. Robustness is studied by measuring the luminescence of (single) NPs after various cycles of electron beam exposure. The gold-core rhodamine B-labelled silica NPs and QDs are quenched after a single exposure to 60 ke − nm –2 with an energy of 120 keV, while Y 2 O 3 :Eu 3+ NPs are robust and still show luminescence after five doses of 60 ke − nm –2 . In addition, the luminescence intensity of Y 2 O 3 :Eu 3+ NPs is investigated as function of electron dose for various electron fluxes. The luminescence intensity initially drops to a constant value well above the single particle detection limit. The intensity loss does not depend on the electron flux, but on the total electron dose. The results indicate that Y 2 O 3 :Eu 3+ NPs are promising as robust fiducial marker in CLEM. Lay Description: Luminescent particles are used as fiducial markers in correlative light and electron microscopy (CLEM) to enable accurate overlaying of fluorescence and electron microscopy images. The currently used fiducial markers, e.g. dyes and quantum dots, loose their luminescence after exposure to the electron beam of the electron microscope. This limits their use in CLEM, since samples have to be studied with light microscopy before the sample can be studied with electron microscopy. Robust fiducial markers, i.e. luminescent labels that can withstand electron exposure, are interesting because of recent developments in integrated CLEM microscopes. Also nonintegrated CLEM setups may benefit from such fiducial markers. Such markers would allow for switching back to fluorescence imaging after the recording of electron microscopy imaging and are not available yet. Here, we investigate the robustness of various luminescent nanoparticles (NPs) that have good contrast in electron microscopy; dye-labelled silica particles, quantum dots and lanthanide-doped inorganic particles. Robustness is studied by measuring the luminescence of (single) NPs after various cycles of electron beam exposure. The dye-labelled silica NPs and QDs are quenched after a single exposure to 60 ke − nm –2 with an energy of 120 keV, while lanthanide-doped inorganic NPs are robust and still show luminescence after five doses of 60 ke − nm –2 . In addition, the luminescence intensity of lanthanide-doped inorganic NPs is investigated as function of electron dose for various electron fluxes. The luminescence intensity initially drops to a constant value well above the single particle detection limit. The intensity loss does not depend on the electron flux, but on the total electron dose. The results indicate that lanthanide-doped NPs are promising as robust fiducial marker in CLEM. © 2019 The Authors. Journal of Microscopy published by JohnWiley & Sons Ltd on behalf of Royal Microscopical Society.},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
Mohammadian, Sajjad; Fokkema, Jantina; Agronskaia, Alexandra V; Liv, N; de Heus, C; van Donselaar, E; Blab, Gerhard A.; Klumperman, J; Gerritsen, Hans C
High accuracy, fiducial marker-based image registration of correlative microscopy images Journal Article
In: Scientific Reports, vol. 9, no. 1, 2019.
@article{mohammadian_high_2019,
title = {High accuracy, fiducial marker-based image registration of correlative microscopy images},
author = {Sajjad Mohammadian and Jantina Fokkema and Alexandra V Agronskaia and N Liv and C de Heus and E van Donselaar and Gerhard A. Blab and J Klumperman and Hans C Gerritsen},
doi = {10.1038/s41598-019-40098-4},
year = {2019},
date = {2019-01-01},
journal = {Scientific Reports},
volume = {9},
number = {1},
abstract = {Fluorescence microscopy (FM) and electron microscopy (EM) are complementary techniques. FM affords examination of large fields of view and identifying regions of interest but has a low resolution. EM exhibits excellent resolution over a limited field of view. The combination of these two techniques, correlative microscopy, received considerable interest in the past years and has proven its potential in biology and material science. Accurate correlation of FM and EM images is, however, challenging due to the differences in contrast mechanism, size of field of view and resolution. We report an accurate, fast and robust method to correlate FM and EM images using low densities of fiducial markers. Here, 120 nm diameter fiducial markers consisting of fluorescently labelled silica coated gold nanoparticles are used. The method relies on recording FM, low magnification EM and high magnification EM images. Two linear transformation matrices are constructed, FM to low magnification EM and low magnification EM to high magnification EM. Combination of these matrices results in a high accuracy transformation of FM to high magnification EM coordinates. The method was tested using two different transmission electron microscopes and different Tokuyasu and Lowicryl sections. The overall accuracy of the correlation method is high, 5–30 nm. © 2019, The Author(s).},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
2018
Fokkema, Jantina; Fermie, Job; Liv, Nalan; van den Heuvel, Dave J.; Konings, Tom O. M.; Blab, Gerhard A.; Meijerink, Andries; Klumperman, Judith; Gerritsen, Hans C.
Fluorescently Labelled Silica Coated Gold Nanoparticles as Fiducial Markers for Correlative Light and Electron Microscopy Journal Article
In: Scientific Reports, vol. 8, no. 1, pp. 13625, 2018.
@article{Fokkema2018,
title = {Fluorescently Labelled Silica Coated Gold Nanoparticles as Fiducial Markers for Correlative Light and Electron Microscopy},
author = {Jantina Fokkema and Job Fermie and Nalan Liv and Dave J. van den Heuvel and Tom O. M. Konings and Gerhard A. Blab and Andries Meijerink and Judith Klumperman and Hans C. Gerritsen},
url = {https://doi.org/10.1038/s41598-018-31836-1},
doi = {10.1038/s41598-018-31836-1},
year = {2018},
date = {2018-09-11},
journal = {Scientific Reports},
volume = {8},
number = {1},
pages = {13625},
abstract = {In this work, gold nanoparticles coated with a fluorescently labelled (rhodamine B) silica shell are presented as fiducial markers for correlative light and electron microscopy (CLEM). The synthesis of the particles is optimized to obtain homogeneous, spherical core-shell particles of arbitrary size. Next, particles labelled with different fluorophore densities are characterized to determine under which conditions bright and (photo)stable particles can be obtained. 2 and 3D CLEM examples are presented where optimized particles are used for correlation. In the 2D example, fiducials are added to a cryosection of cells whereas in the 3D example cells are imaged after endocytosis of the fiducials. Both examples demonstrate that the particles are clearly visible in both modalities and can be used for correlation. Additionally, the recognizable core-shell structure of the fiducials proves to be very powerful in electron microscopy: it makes it possible to irrefutably identify the particles and makes it easy to accurately determine the center of the fiducials.},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
Fermie, Job; Liv, Nalan; ten Brink, Corlinda; van Donselaar, Elly G.; Müller, Wally H.; Schieber, Nicole L.; Schwab, Yannick; Gerritsen, Hans C.; Klumperman, Judith
Single organelle dynamics linked to 3D structure by correlative live-cell imaging and 3D electron microscopy Journal Article
In: Traffic, vol. 19, no. 5, pp. 354-369, 2018.
@article{fermie_CLEM,
title = {Single organelle dynamics linked to 3D structure by correlative live-cell imaging and 3D electron microscopy},
author = { Job Fermie and Nalan Liv and Corlinda ten Brink and Elly G. van Donselaar and Wally H. Müller and Nicole L. Schieber and Yannick Schwab and Hans C. Gerritsen and Judith Klumperman},
url = {https://onlinelibrary.wiley.com/doi/abs/10.1111/tra.12557},
doi = {10.1111/tra.12557},
year = {2018},
date = {2018-02-16},
journal = {Traffic},
volume = {19},
number = {5},
pages = {354-369},
abstract = {Live-cell correlative light-electron microscopy (live-cell-CLEM) integrates live movies with the corresponding electron microscopy (EM) image, but a major challenge is to relate the dynamic characteristics of single organelles to their 3-dimensional (3D) ultrastructure. Here, we introduce focused ion beam scanning electron microscopy (FIB-SEM) in a modular live-cell-CLEM pipeline for a single organelle CLEM. We transfected cells with lysosomal-associated membrane protein 1-green fluorescent protein (LAMP-1-GFP), analyzed the dynamics of individual GFP-positive spots, and correlated these to their corresponding fine-architecture and immediate cellular environment. By FIB-SEM we quantitatively assessed morphological characteristics, like number of intraluminal vesicles and contact sites with endoplasmic reticulum and mitochondria. Hence, we present a novel way to integrate multiple parameters of subcellular dynamics and architecture onto a single organelle, which is relevant to address biological questions related to membrane trafficking, organelle biogenesis and positioning. Furthermore, by using CLEM to select regions of interest, our method allows for targeted FIB-SEM, which significantly reduces time required for image acquisition and data processing.},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
Xia, Cheng-Hui; Winckelmans, N.; Prins, P. T.; Bals, S.; Gerritsen, Hans C.; Donega, Celso De Mello
Near-Infrared-Emitting CuInS2/ZnS Dot-in-Rod Colloidal Heteronanorods by Seeded Growth Journal Article
In: Journal of the American Chemical Society, vol. 140, no. 17, pp. 5755-5763, 2018, (cited By 1).
@article{Xia20185755,
title = {Near-Infrared-Emitting CuInS2/ZnS Dot-in-Rod Colloidal Heteronanorods by Seeded Growth},
author = { Cheng-Hui Xia and N. Winckelmans and P.T. Prins and S. Bals and Hans C. Gerritsen and Celso De Mello Donega},
url = {https://www.scopus.com/inward/record.uri?eid=2-s2.0-85045217473&doi=10.1021%2fjacs.8b01412&partnerID=40&md5=8e0bd7ee2930338cdc574ced9a3b77ca},
doi = {10.1021/jacs.8b01412},
year = {2018},
date = {2018-01-01},
journal = {Journal of the American Chemical Society},
volume = {140},
number = {17},
pages = {5755-5763},
abstract = {Synthesis protocols for anisotropic CuInX2 (X = S, Se, Te)-based heteronanocrystals (HNCs) are scarce due to the difficulty in balancing the reactivities of multiple precursors and the high solid-state diffusion rates of the cations involved in the CuInX2 lattice. In this work, we report a multistep seeded growth synthesis protocol that yields colloidal wurtzite CuInS2/ZnS dot core/rod shell HNCs with photoluminescence in the NIR (∼800 nm). The wurtzite CuInS2 NCs used as seeds are obtained by topotactic partial Cu+ for In3+ cation exchange in template Cu2-xS NCs. The seed NCs are injected in a hot solution of zinc oleate and hexadecylamine in octadecene, 20 s after the injection of sulfur in octadecene. This results in heteroepitaxial growth of wurtzite ZnS primarily on the Sulfur-terminated polar facet of the CuInS2 seed NCs, the other facets being overcoated only by a thin (∼1 monolayer) shell. The fast (∼21 nm/min) asymmetric axial growth of the nanorod proceeds by addition of [ZnS] monomer units, so that the polarity of the terminal (002) facet is preserved throughout the growth. The delayed injection of the CuInS2 seed NCs is crucial to allow the concentration of [ZnS] monomers to build up, thereby maximizing the anisotropic heteroepitaxial growth rates while minimizing the rates of competing processes (etching, cation exchange, alloying). Nevertheless, a mild etching still occurred, likely prior to the onset of heteroepitaxial overgrowth, shrinking the core size from 5.5 to ∼4 nm. The insights provided by this work open up new possibilities in designing multifunctional Cu-chalcogenide based colloidal heteronanocrystals. © 2018 American Chemical Society.},
note = {cited By 1},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
Hendriks, F. C.; Mohammadian, Sajjad; Ristanović, Z.; Kalirai, S.; Meirer, F.; Vogt, E. T. C.; Bruijnincx, P. C. A.; Gerritsen, Hans C.; Weckhuysen, B. M.
In: Angewandte Chemie - International Edition, vol. 57, no. 1, pp. 257-261, 2018, (cited By 3).
@article{Hendriks2018257,
title = {Integrated Transmission Electron and Single-Molecule Fluorescence Microscopy Correlates Reactivity with Ultrastructure in a Single Catalyst Particle},
author = { F.C. Hendriks and Sajjad Mohammadian and Z. Ristanović and S. Kalirai and F. Meirer and E.T.C. Vogt and P.C.A. Bruijnincx and Hans C. Gerritsen and B.M. Weckhuysen},
url = {https://www.scopus.com/inward/record.uri?eid=2-s2.0-85034657596&doi=10.1002%2fanie.201709723&partnerID=40&md5=5ec7400275144d61e7be3fb318585745},
doi = {10.1002/anie.201709723},
year = {2018},
date = {2018-01-01},
journal = {Angewandte Chemie - International Edition},
volume = {57},
number = {1},
pages = {257-261},
abstract = {Establishing structure–activity relationships in complex, hierarchically structured nanomaterials, such as fluid catalytic cracking (FCC) catalysts, requires characterization with complementary, correlated analysis techniques. An integrated setup has been developed to perform transmission electron microscopy (TEM) and single-molecule fluorescence (SMF) microscopy on such nanostructured samples. Correlated structure–reactivity information was obtained for 100 nm thin, microtomed sections of a single FCC catalyst particle using this novel SMF-TEM high-resolution combination. High reactivity in a thiophene oligomerization probe reaction correlated well with TEM-derived zeolite locations, while matrix components, such as clay and amorphous binder material, were found not to display activity. Differences in fluorescence intensity were also observed within and between distinct zeolite aggregate domains, indicating that not all zeolite domains are equally active. © 2017 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA.},
note = {cited By 3},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
Xia, Cheng-Hui; Wu, W.; Yu, T.; Xie, X.; Oversteeg, C. V.; Gerritsen, Hans C.; Donega, Celso De Mello
Size-Dependent Band-Gap and Molar Absorption Coefficients of Colloidal CuInS2 Quantum Dots Journal Article
In: ACS Nano, 2018, (cited By 0; Article in Press).
@article{Xia2018b,
title = {Size-Dependent Band-Gap and Molar Absorption Coefficients of Colloidal CuInS2 Quantum Dots},
author = { Cheng-Hui Xia and W. Wu and T. Yu and X. Xie and C.V. Oversteeg and Hans C. Gerritsen and Celso De Mello Donega},
url = {https://www.scopus.com/inward/record.uri?eid=2-s2.0-85052281980&doi=10.1021%2facsnano.8b03641&partnerID=40&md5=1cd5167c14bae03656197e6bb145296f},
doi = {10.1021/acsnano.8b03641},
year = {2018},
date = {2018-01-01},
journal = {ACS Nano},
abstract = {The knowledge of the quantum dot (QD) concentration in a colloidal suspension and the quantitative understanding of the size-dependence of the band gap of QDs are of crucial importance from both applied and fundamental viewpoints. In this work, we investigate the size-dependence of the optical properties of nearly spherical wurtzite (wz) CuInS2 (CIS) QDs in the 2.7 to 6.1 nm diameter range (polydispersity ≤10%). The QDs are synthesized by partial Cu+ for In3+ cation exchange in template Cu2-xS NCs, which yields CIS QDs with very small composition variations (In/Cu= 0.91±0.11), regardless of their sizes. These well-defined QDs are used to investigate the size dependence of the band gap of wz CIS QDs. A sizing curve is also constructed for chalcopyrite CIS QDs by collecting and reanalyzing literature data. We observe that both sizing curves follow primarily a 1/d dependence. Moreover, the molar absorption coefficients and the absorption cross-section per CIS formula unit, both at 3.1 eV and at the band gap, are analyzed. The results demonstrate that the molar absorption coefficients of CIS QDs follow a power law at the first exciton transition energy (ϵE1)=5208 d^2.45), and scale with the QD volume at 3.1 eV. This latter observation implies that the absorption cross-section per unit cell at 3.1 eV is size-independent, and therefore can be estimated from bulk optical constants. These results also demonstrate that the molar absorption coefficients at 3.1 eV are more reliable for analytical purposes, since they are less sensitive to size and shape dispersion. © 2018 American Chemical Society.},
note = {cited By 0; Article in Press},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
van Hest, Jacobine J. H. A.; Blab, Gerhard A.; Gerritsen, Hans C.; de Mello Donega, Celso; Meijerink, Andries
The Role of a Phonon Bottleneck in Relaxation Processes for Ln-Doped NaYF4 Nanocrystals Journal Article
In: The Journal of Physical Chemistry C, vol. 122, no. 7, pp. 3985–3993, 2018, ISSN: 1932-7447.
@article{van_hest_role_2018,
title = {The Role of a Phonon Bottleneck in Relaxation Processes for Ln-Doped NaYF4 Nanocrystals},
author = { Jacobine J. H. A. van Hest and Gerhard A. Blab and Hans C. Gerritsen and Celso de Mello Donega and Andries Meijerink},
url = {https://doi.org/10.1021/acs.jpcc.7b11171},
doi = {10.1021/acs.jpcc.7b11171},
issn = {1932-7447},
year = {2018},
date = {2018-01-01},
urldate = {2018-09-11},
journal = {The Journal of Physical Chemistry C},
volume = {122},
number = {7},
pages = {3985--3993},
abstract = {The localized inner 4f shell transitions of lanthanide ions are largely independent of the local surroundings. The luminescence properties of Ln3+ ions doped into nanocrystals (NCs) are therefore similar to those in bulk crystals. Quantum size effects, responsible for the unique size-dependent luminescence of semiconductor NCs, are generally assumed not to influence the optical properties of Ln3+-doped insulator NCs. However, phonon confinement effects have been reported to hamper relaxation between closely spaced Stark levels in Ln3+-doped NCs. At cryogenic temperatures emission and excitation from higher Stark levels was observed for Ln3+ ions in NCs only and were explained by a cutoff in the acoustic phonon spectrum. Relaxation would be inhibited as no resonant low energy (long wavelength) acoustic phonon modes can exist in nanometer sized crystals, and this prevents relaxation by direct phonon emission between closely spaced Stark levels. This phenomenon is known as a phonon bottleneck. Here, we investigate the role of phonon confinement in Ln-doped NCs. High resolution emission spectra at temperatures down to 2.2 K are reported for various Ln3+ ions (Er3+, Yb3+, Eu3+) doped into monodisperse 10 nm NaYF4 NCs and compared with spectra for bulk (microcrystalline) material. Contrary to previous reports, we find no evidence for phonon bottleneck effects in the emission spectra. Emission from closely spaced higher Stark levels is observed only at high excitation powers and is explained by laser heating. The present results indicate that previously reported effects in NCs may not be caused by phonon confinement.},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
2017
van Hest, Jacobine J. H. A.; Blab, Gerhard A.; Gerritsen, Hans C.; de Mello-Donega, Celso; Meijerink, Andries
Probing the Influence of Disorder on Lanthanide Luminescence Using Eu-Doped LaPO4 Nanoparticles Journal Article
In: The Journal of Physical Chemistry C, vol. 121, no. 35, pp. 19373-19382, 2017.
@article{doi:10.1021/acs.jpcc.7b06549,
title = {Probing the Influence of Disorder on Lanthanide Luminescence Using Eu-Doped LaPO4 Nanoparticles},
author = { Jacobine J.H.A. van Hest and Gerhard A. Blab and Hans C. Gerritsen and Celso de Mello-Donega and Andries Meijerink},
url = {http://dx.doi.org/10.1021/acs.jpcc.7b06549},
doi = {10.1021/acs.jpcc.7b06549},
year = {2017},
date = {2017-01-01},
journal = {The Journal of Physical Chemistry C},
volume = {121},
number = {35},
pages = {19373-19382},
abstract = {Lanthanide-doped nanocrystals (NCs) differ from their bulk counterparts due to their large surface to volume ratio. It is generally assumed that the optical properties are not affected by size effects as electronic transitions occur within the well-shielded 4f shell of the lanthanide dopant ions. However, defects and disorder in the surface layer can affect the luminescence properties. Trivalent europium is a suitable ion to investigate the subtle influence of the surface, because of its characteristic luminescence and high sensitivity to the local environment. Here, we investigate the influence of disorder in NCs on the optical properties of lanthanide dopants by studying the inhomogeneous linewidth, emission intensity ratios, and luminescence decay curves for LaPO4:Eu3+ samples of different sizes (4 nm to bulk) and core–shell configurations (core, core–isocrystalline shell, and core–silica shell). We show that the emission linewidths increase strongly for NCs. The ratio of the intensities of the forced electric dipole (ED) and magnetic dipole (MD) transitions, a measure for the local symmetry distortion around Eu3+ ions, is higher for samples with a large fraction of Eu3+ ions close to the surface. Finally, we present luminescence decay curves revealing an increased nonradiative decay rate for Eu3+ in NCs. The effects are strongest in core and core–silica shell NCs and can be reduced by growth of an isocrystalline LaPO4 shell. The present systematic study provides quantitative insight into the role of surface disorder on the optical properties of lanthanide-doped NCs. These insights are important in emerging applications of lanthanide-doped nanocrystals.},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
Xia, Cheng-Hui; Meeldijk, Johannes D.; Gerritsen, Hans C.; de Mello-Donega, Celso
Highly Luminescent Water-Dispersible NIR-Emitting Wurtzite CuInS2/ZnS Core/Shell Colloidal Quantum Dots Journal Article
In: Chemistry of Materials, vol. 29, no. 11, pp. 4940-4951, 2017.
@article{Xia20174940,
title = {Highly Luminescent Water-Dispersible NIR-Emitting Wurtzite CuInS2/ZnS Core/Shell Colloidal Quantum Dots},
author = { Cheng-Hui Xia and Johannes D. Meeldijk and Hans C. Gerritsen and Celso de Mello-Donega},
url = {https://www.scopus.com/inward/record.uri?eid=2-s2.0-85020755702&doi=10.1021%2facs.chemmater.7b01258&partnerID=40&md5=e2ad969aafe4216675cf983c833eb6b0},
doi = {10.1021/acs.chemmater.7b01258},
year = {2017},
date = {2017-01-01},
journal = {Chemistry of Materials},
volume = {29},
number = {11},
pages = {4940-4951},
abstract = {Copper indium sulfide (CIS) quantum dots (QDs) are attractive as labels for biomedical imaging, since they have large absorption coefficients across a broad spectral range, size- and composition-tunable photoluminescence from the visible to the near-infrared, and low toxicity. However, the application of NIR-emitting CIS QDs is still hindered by large size and shape dispersions and low photoluminescence quantum yields (PLQYs). In this work, we develop an efficient pathway to synthesize highly luminescent NIR-emitting wurtzite CIS/ZnS QDs, starting from template Cu2-xS nanocrystals (NCs), which are converted by topotactic partial Cu+ for In3+ exchange into CIS NCs. These NCs are subsequently used as cores for the overgrowth of ZnS shells (≤1 nm thick). The CIS/ZnS core/shell QDs exhibit PL tunability from the first to the second NIR window (750-1100 nm), with PLQYs ranging from 75% (at 820 nm) to 25% (at 1050 nm), and can be readily transferred to water upon exchange of the native ligands for mercaptoundecanoic acid. The resulting water-dispersible CIS/ZnS QDs possess good colloidal stability over at least 6 months and PLQYs ranging from 39% (at 820 nm) to 6% (at 1050 nm). These PLQYs are superior to those of commonly available water-soluble NIR-fluorophores (dyes and QDs), making the hydrophilic CIS/ZnS QDs developed in this work promising candidates for further application as NIR emitters in bioimaging. The hydrophobic CIS/ZnS QDs obtained immediately after the ZnS shelling are also attractive as fluorophores in luminescent solar concentrators. © 2017 American Chemical Society.},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
Thomas, Giju; Tuk, Bastiaan; Song, Ji Ying; Truong, Hoa H.; Gerritsen, Hans C.; de Gruijl, Frank R.; Sterenborg, Henricus J. C. M.
In: Laboratory Animals, vol. 51, no. 1, pp. 24-35, 2017.
@article{Thomas201724,
title = {Studying skin tumourigenesis and progression in immunocompetent hairless SKH1-hr mice using chronic 7,12-dimethylbenz(a)anthracene topical applications to develop a useful experimental skin cancer model},
author = {Giju Thomas and Bastiaan Tuk and Ji Ying Song and Hoa H. Truong and Hans C. Gerritsen and Frank R. de Gruijl and Henricus J.C.M. Sterenborg},
url = {https://www.scopus.com/inward/record.uri?eid=2-s2.0-85014446283&doi=10.1177%2f0023677216637305&partnerID=40&md5=86fdf0245e203bd2db167d9b507f5661},
doi = {10.1177/0023677216637305},
year = {2017},
date = {2017-01-01},
journal = {Laboratory Animals},
volume = {51},
number = {1},
pages = {24-35},
abstract = {Previous studies have established that 7,12-dimethylbenz(a)anthracene (DMBA) can initiate skin tumourigenesis in conventional furred mouse models by acting on hair follicle stem cells. However, further cancer progression depends on repeated applications of tumour promoter agents. This study evaluated the timeline involved in skin tumourigenesis and progression in immunocompetent hairless SKH1-hr mice with dysfunctional hair follicles using only DMBA with no additional tumour promoter agents. The results showed that topical application of 30 μg (117 nmol) of DMBA over the back and flank regions of the mouse once a week and 15 μg (58.5 nmol) twice a week produced skin tumours after 7–8 weeks. However, by week 14 a heavy benign tumour load required the mice to be euthanized. Lowering the DMBA dose to 15 μg (58.5 nmol) once a week produced tumours more slowly and allowed the mice to be studied for a longer period to week 23. This lowdose DMBA regimen yielded a high percentage of malignant tumours (58.8%) after 23 weekly applications. Additionally DMBA-treated skin showed an increase in mean epidermal thickness in comparison to untreated and acetone-treated skin. Despite the aberrant hair follicles in SKH1-hr mice, this chemically driven skin cancer model in hairless mice can serve as a suitable alternative to the ultraviolet-induced skin cancer models and can be reliably replicated as demonstrated by both the pilot and main experiments. © The Author(s) 2016.},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
2016
van Hest, Jacobine J. H. A.; Blab, Gerhard A.; Gerritsen, Hans C.; de Mello-Donega, Celso; Meijerink, Andries
Incorporation of Ln-Doped LaPO4 Nanocrystals as Luminescent Markers in Silica Nanoparticles Journal Article
In: Nanoscale Research Letters, vol. 11, no. 1, 2016, ISSN: 1931-7573, 1556-276X.
@article{van_hest_incorporation_2016,
title = {Incorporation of Ln-Doped LaPO4 Nanocrystals as Luminescent Markers in Silica Nanoparticles},
author = {Jacobine J.H.A. van Hest and Gerhard A. Blab and Hans C. Gerritsen and Celso de Mello-Donega and Andries Meijerink},
url = {http://nanoscalereslett.springeropen.com/articles/10.1186/s11671-016-1465-y},
doi = {10.1186/s11671-016-1465-y},
issn = {1931-7573, 1556-276X},
year = {2016},
date = {2016-01-01},
urldate = {2016-07-11},
journal = {Nanoscale Research Letters},
volume = {11},
number = {1},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
2015
de Jonge, Niels; Blab, Gerhard A.; Karreman, Matthia A.; Agronskaia, Alexandra V.; Gerritsen, Hans C.
Advances in Imaging and Electron Physics (contr.) Book Chapter
In: Hawkes, Peter W. (Ed.): vol. 190, Chapter 1, pp. 1–102, 978-0-12-802380-8 , 225 Wyman Street, Waltham, MA 02451, USA 525 B Street, Suite 1800, San Diego, CA 92101-4495, USA 125 London Wall, London, EC2Y 5AS, UK The Boulevard, Langford Lane, Kidlington, Oxford OX5 1GB, UK, 2015, ISBN: 978-0-12-802380-8.
@inbook{deJonge2015,
title = {Advances in Imaging and Electron Physics (contr.)},
author = {Niels de Jonge and Gerhard A. Blab and Matthia A. Karreman and Alexandra V. Agronskaia and Hans C. Gerritsen},
editor = {Peter W. Hawkes},
doi = {10.1016/bs.aiep.2015.02.004},
isbn = {978-0-12-802380-8},
year = {2015},
date = {2015-05-18},
volume = {190},
pages = {1--102},
publisher = {978-0-12-802380-8 },
address = {225 Wyman Street, Waltham, MA 02451, USA 525 B Street, Suite 1800, San Diego, CA 92101-4495, USA 125 London Wall, London, EC2Y 5AS, UK The Boulevard, Langford Lane, Kidlington, Oxford OX5 1GB, UK},
chapter = {1},
series = {Advances in Imaging and Electron Physics},
abstract = {This chapter contains the extended abstracts of the second conference on in situ and correlative electron microscopy (CISCEM 2014), held October 14–15, 2014, in Saarbrücken, Germany. The conference was housed at the INM-Leibniz Institute for New Materials. The aim of the conference was to bring together an interdisciplinary group of scientists from the fields of biology, materials science, chemistry, and physics to discuss future directions of electron microscopy research. The topics of the different sessions were correlative and in situ electron microscopy in biology, in situ observations of biomineralization processes, designing in situ experiments, high-temperature and other experiments, and in situ transmission electron microscopy of catalytic nanoparticles. A corporate session was also held.},
type = {Academic Press},
keywords = {},
pubstate = {published},
tppubtype = {inbook}
}
Zuckermann, Martin J.; Angstmann, Christopher N.; Schmitt, Regina; Blab, Gerhard A.; Bromley, Elizabeth H. C.; Forde, Nancy R.; Linke, Heiner; Curmi, Paul M. G.
Motor properties from persistence: a linear molecular walker lacking spatial and temporal asymmetry Journal Article
In: New Journal of Phyiscs, vol. 17, pp. 055017, 2015.
@article{Zuckermann2015,
title = {Motor properties from persistence: a linear molecular walker lacking spatial and temporal asymmetry},
author = {Martin J. Zuckermann and Christopher N. Angstmann and Regina Schmitt and Gerhard A. Blab and Elizabeth H.C. Bromley and Nancy R. Forde and Heiner Linke and Paul M.G. Curmi},
url = {http://iopscience.iop.org/1367-2630/17/5/055017/},
doi = {10.1088/1367-2630/17/5/055017},
year = {2015},
date = {2015-05-05},
journal = {New Journal of Phyiscs},
volume = {17},
pages = {055017},
abstract = {The stepping direction of linear molecular motors is usually defined by a spatial asymmetry of the motor, its track, or both. Here we present a model for a molecular walker that undergoes biased directional motion along a symmetric track in the presence of a temporally symmetric chemical cycle. Instead of using asymmetry, directionality is achieved by persistence. At small load force the walker can take on average thousands of steps in a given direction until it stochastically reverses direction. We discuss a specific experimental implementation of a synthetic motor based on this design and find, using Langevin and Monte Carlo simulations, that a realistic walker can work against load forces on the order of picoNewtons with an efficiency of ~18%, comparable to that of kinesin. In principle, the walker can be turned into a permanent motor by externally monitoring the walker's momentary direction of motion, and using feedback to adjust the direction of a load force. We calculate the thermodynamic cost of using feedback to enhance motor performance in terms of the Shannon entropy, and find that it reduces the efficiency of a realistic motor only marginally. We discuss the implications for natural protein motor performance in the context of the strong performance of this design based only on a thermal ratchet.},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
Jose, Jissy; Blab, Gerhard A.; van Blaaderen, Alfons; Imhof, Arnout
Jammed elastic shells – a 3D experimental soft frictionless granular system Journal Article
In: Soft Matter, vol. 11, no. 9, pp. 1800-1813, 2015.
@article{vanImhof2015,
title = {Jammed elastic shells – a 3D experimental soft frictionless granular system },
author = {Jissy Jose and Gerhard A. Blab and Alfons van Blaaderen and Arnout Imhof},
url = {http://pubs.rsc.org/en/content/articlelanding/2015/sm/c4sm02098g},
doi = {10.1039/C4SM02098G },
year = {2015},
date = {2015-03-07},
journal = {Soft Matter},
volume = {11},
number = {9},
pages = {1800-1813},
abstract = {We present a new experimental system of monodisperse, soft, frictionless, fluorescent labeled elastic shells for the characterization of structure, universal scaling laws and force networks in 3D jammed matter. The elastic shells in a jammed packing are deformed in such a way that at each contact one of the shells buckles with a dimple and the other remain spherical, closely resembling overlapping spheres. Using confocal microscopy, we obtained 3D stacks of images of shells at different volume fractions which were subsequently processed in ImageJ software to find their coordinates. The determination of 3D coordinates involved three steps: locating the edges of shells in all 2D slices, analyzing their shape and subsequently finding their 2D coordinates, and finally determining their 3D centers by grouping the corresponding 2D coordinates. From this analysis routine we obtained particle coordinates with sub-pixel accuracy. In a contact pair we also identified the shell that underwent buckling forming a dimple by analyzing the intensity profile of a line that connects the centers of particle pairs. The amorphous structure of the packing was analyzed as a function of distance to the jamming threshold by investigating the radial distribution function, bond order parameters, contact numbers and the number of dimples per particle (buckling number), which is a unique property of this system. We find that the power law scaling of the contact number with excess volume fraction deviated from theoretical and computer simulation predictions. In addition, the buckling number also showed a similar scaling as that of the contact number with distance to the jamming transition.},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
van Dijk, Lourens; Paetzold, Ulrich W.; Blab, Gerhard A.; Schropp, Ruud E. I.; di Vece, Marcel
3D-printed external light trap for solar cells Journal Article
In: Progress in Photovoltaics: Research and Applications, pp. n/a–n/a, 2015, ISSN: 1099-159X, (pip.2702).
@article{PIP:PIP2702,
title = {3D-printed external light trap for solar cells},
author = {Lourens van Dijk and Ulrich W. Paetzold and Gerhard A. Blab and Ruud E.I. Schropp and Marcel di Vece},
url = {http://dx.doi.org/10.1002/pip.2702},
doi = {10.1002/pip.2702},
issn = {1099-159X},
year = {2015},
date = {2015-01-01},
journal = {Progress in Photovoltaics: Research and Applications},
pages = {n/a--n/a},
abstract = {We present a universally applicable 3D-printed external light trap for enhanced absorption in solar cells. The macroscopic external light trap is placed at the sun-facing surface of the solar cell and retro-reflects the light that would otherwise escape. The light trap consists of a reflective parabolic concentrator placed on top of a reflective cage. Upon placement of the light trap, an improvement of 15% of both the photocurrent and the power conversion efficiency in a thin-film nanocrystalline silicon (nc-Si:H) solar cell is measured. The trapped light traverses the solar cell several times within the reflective cage thereby increasing the total absorption in the cell. Consequently, the trap reduces optical losses and enhances the absorption over the entire spectrum. The components of the light trap are 3D printed and made of smoothened, silver-coated thermoplastic. In contrast to conventional light trapping methods, external light trapping leaves the material quality and the electrical properties of the solar cell unaffected. To explain the theoretical operation of the external light trap, we introduce a model that predicts the absorption enhancement in the solar cell by the external light trap. The corresponding calculated path length enhancement shows good agreement with the empirically derived value from the opto-electrical data of the solar cell. Moreover, we analyze the influence of the angle of incidence on the parasitic absorptance to obtain full understanding of the trap performance.Copyright © 2015 © 2015 The Authors. Progress in Photovoltaics: Research and Applications published by John Wiley & Sons Ltd.},
note = {pip.2702},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
2014
Thomas, Giju; van Voskuilen, Johan; Gerritsen, Hans C.; Sterenborg, Henricus J. C. M.
In: J. Photochem. Photobiol. B, Biol., vol. 141, pp. 128–138, 2014, ([DOI:hrefhttp://dx.doi.org/10.1016/j.jphotobiol.2014.08.02510.1016/j.jphotobiol.2014.08.025] [PubMed:hrefhttp://www.ncbi.nlm.nih.gov/pubmed/2546366025463660]).
@article{Thomas2014,
title = {Advances and challenges in label-free nonlinear optical imaging using two-photon excitation fluorescence and second harmonic generation for cancer research},
author = { Giju Thomas and Johan van Voskuilen and Hans C. Gerritsen and Henricus J.C.M. Sterenborg},
doi = {10.1016/j.jphotobiol.2014.08.02510.1016},
year = {2014},
date = {2014-12-01},
journal = {J. Photochem. Photobiol. B, Biol.},
volume = {141},
pages = {128--138},
abstract = {Nonlinear optical imaging (NLOI) has emerged to be a promising tool for bio-medical imaging in recent times. Among the various applications of NLOI, its utility is the most significant in the field of pre-clinical and clinical cancer research. This review begins by briefly covering the core principles involved in NLOI, such as two-photon excitation fluorescence (TPEF) and second harmonic generation (SHG). Subsequently, there is a short description on the various cellular components that contribute to endogenous optical fluorescence. Later on the review deals with its main theme--the challenges faced during label-free NLO imaging in translational cancer research. While this review addresses the accomplishment of various label-free NLOI based studies in cancer diagnostics, it also touches upon the limitations of the mentioned studies. In addition, areas in cancer research that need to be further investigated by label-free NLOI are discussed in a latter segment. The review eventually concludes on the note that label-free NLOI has and will continue to contribute richly in translational cancer research, to eventually provide a very reliable, yet minimally invasive cancer diagnostic tool for the patient.},
note = {[DOI:hrefhttp://dx.doi.org/10.1016/j.jphotobiol.2014.08.02510.1016/j.jphotobiol.2014.08.025] [PubMed:hrefhttp://www.ncbi.nlm.nih.gov/pubmed/2546366025463660]},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
Thomas, Giju; van Voskuilen, Johan; Truong, Hoa H.; Gerritsen, Hans C.; Sterenborg, Henricus J. C. M.
In vivo nonlinear optical imaging to monitor early microscopic changes in a murine cutaneous squamous cell carcinoma model Journal Article
In: J Biophotonics, vol. 9999, no. 9999, 2014.
@article{pmid25319484,
title = {In vivo nonlinear optical imaging to monitor early microscopic changes in a murine cutaneous squamous cell carcinoma model},
author = {Giju Thomas and Johan van Voskuilen and Hoa H. Truong and Hans C. Gerritsen and Henricus J.C.M. Sterenborg},
doi = {10.1002/jbio.201400074},
year = {2014},
date = {2014-10-15},
journal = {J Biophotonics},
volume = {9999},
number = {9999},
abstract = {Early detection of cutaneous squamous cell carcinoma (cSCC) can enable timely therapeutic and preventive interventions for patients. In this study, in vivo nonlinear optical imaging (NLOI) based on two-photon excitation fluorescence (TPEF) and second harmonic generation (SHG), was used to non-invasively detect microscopic changes occurring in murine skin treated topically with 7,12-dimethylbenz(a)anthracene (DMBA). The optical microscopic findings and the measured TPEF-SHG index show that NLOI was able to clearly detect early cytostructural changes in DMBA treated skin that appeared clinically normal. This suggests that in vivo NLOI could be a non-invasive tool to monitor early signs of cSCC. In vivo axial NLOI scans of normal murine skin (upper left), murine skin with preclinical hyperplasia (upper right), early clinical murine skin lesion (lower left) and late or advanced murine skin lesion (lower right).},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
Thomas, Giju; Nadiarnykh, Oleg; van Voskuilen, Johan; Hoy, Christopher L.; Gerritsen, Hans C.; Sterenborg, Henricus J. C. M.
Estimating the risk of squamous cell cancer induction in skin following nonlinear optical imaging Journal Article
In: J Biophotonics, vol. 7, no. 7, pp. 492–505, 2014, ([DOI:hrefhttp://dx.doi.org/10.1002/jbio.20120020710.1002/jbio.201200207] [PubMed:hrefhttp://www.ncbi.nlm.nih.gov/pubmed/2340141923401419]).
@article{pmid23401419,
title = {Estimating the risk of squamous cell cancer induction in skin following nonlinear optical imaging},
author = { Giju Thomas and Oleg Nadiarnykh and Johan van Voskuilen and Christopher L. Hoy and Hans C. Gerritsen and Henricus J.C.M. Sterenborg},
year = {2014},
date = {2014-07-01},
journal = {J Biophotonics},
volume = {7},
number = {7},
pages = {492--505},
abstract = {High power femto-second (fs) laser pulses used for in-vivo nonlinear optical (NLO) imaging can form cyclobutane pyrimidine dimers (CPD) in DNA, which may lead to carcinogenesis via subsequent mutations. Since UV radiation from routine sun exposure is the primary source of CPD lesions, we evaluated the risk of CPD-related squamous cell carcinoma (SCC) in human skin due to NLO imaging relative to that from sun exposure. We developed a unique cancer risk model expanding previously published estimation of risk from exposure to continuous wave (CW) laser. This new model showed that the increase in CPD-related SCC in skin from NLO imaging is negligible above that due to regular sun exposure.},
note = {[DOI:hrefhttp://dx.doi.org/10.1002/jbio.20120020710.1002/jbio.201200207] [PubMed:hrefhttp://www.ncbi.nlm.nih.gov/pubmed/2340141923401419]},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
Revalee, Joel D.; Blab, Gerhard A.; Wilson, Henry D.; Kahn, Jason D.; Meiners, Jens Christian
Tethered particle motion reveals that LacI·DNA loops coexist with a competitor-resistant but apparently unlooped conformation Journal Article
In: Biophysical Journal, vol. 106, no. 3, pp. 705-715, 2014, (cited By 1).
@article{Revalee2014705,
title = {Tethered particle motion reveals that LacI·DNA loops coexist with a competitor-resistant but apparently unlooped conformation},
author = { Joel D. Revalee and Gerhard A. Blab and Henry D. Wilson and Jason D. Kahn and Jens Christian Meiners},
url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-84893515191&partnerID=40&md5=b469b5118033e09f75eb18a2f5dee398},
doi = {10.1016/j.bpj.2013.12.024},
year = {2014},
date = {2014-02-04},
journal = {Biophysical Journal},
volume = {106},
number = {3},
pages = {705-715},
abstract = {The lac repressor protein (LacI) efficiently represses transcription of the lac operon in Escherichia coli by binding to two distant operator sites on the bacterial DNA and causing the intervening DNA to form a loop. We employed single-molecule tethered particle motion to observe LacI-mediated loop formation and breakdown in DNA constructs that incorporate optimized operator binding sites and intrinsic curvature favorable to loop formation. Previous bulk competition assays indirectly measured the loop lifetimes in these optimized DNA constructs as being on the order of days; however, we measured these same lifetimes to be on the order of minutes for both looped and unlooped states. In a range of single-molecule DNA competition experiments, we found that the resistance of the LacI-DNA complex to competitive binding is a function of both the operator strength and the interoperator sequence. To explain these findings, we present what we believe to be a new kinetic model of loop formation and DNA competition. In this proposed new model, we hypothesize a new unlooped state in which the unbound DNA-binding domain of the LacI protein interacts nonspecifically with nonoperator DNA adjacent to the operator site at which the second LacI DNA-binding domain is bound. © 2014 Biophysical Society.},
note = {cited By 1},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
Fereidouni, Farzad; Blab, Gerhard A.; Gerritsen, Hans C.
Phasor based analysis of FRET images recorded using spectrally resolved lifetime imaging Journal Article
In: Methods and Applications in Fluorescence, vol. 2, no. 3, pp. 035001, 2014.
@article{2050-6120-2-3-035001,
title = {Phasor based analysis of FRET images recorded using spectrally resolved lifetime imaging},
author = {Farzad Fereidouni and Gerhard A. Blab and Hans C. Gerritsen},
url = {http://stacks.iop.org/2050-6120/2/i=3/a=035001},
year = {2014},
date = {2014-01-01},
journal = {Methods and Applications in Fluorescence},
volume = {2},
number = {3},
pages = {035001},
abstract = {The combined analysis of spectral and lifetime images has the potential to provide more accurate and more detailed information about Förster resonance energy transfer (FRET). We have developed a novel FRET analysis method to analyze images recorded by multispectral lifetime imaging. The new method is based on a phasor approach and facilitates the simultaneous analysis of decay kinetics of donor and acceptor molecules. The method is applicable to both molecules that exhibit a mono-exponential decay and a bi-exponential decay. As an example we show the possibility of extracting the energy transfer efficiency and the fraction of interacting molecules even in the presence of non-interacting molecules. The reliability of the method is investigated by comparing it with conventional FRET-FLIM analyses. We show that, with the same number of detected photons, the spectrally resolved phasor approach provides higher accuracy than other analysis methods; the confidence interval is improved and the FRET efficiency is closer to the real value.},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
2013
Knaus, Helene; Blab, Gerhard A.; van Veluw, G. Jerre; Gerritsen, Hans C.; Wösten, Han A. B.
Label-free fluorescence microscopy in fungi Journal Article
In: Fungal Biology Reviews, no. 0, pp. -, 2013, ISSN: 1749-4613, (in press).
@article{Knaus2013,
title = {Label-free fluorescence microscopy in fungi},
author = {Helene Knaus and Gerhard A. Blab and G. Jerre van Veluw and Hans C. Gerritsen and Han A.B. Wösten},
url = {http://www.sciencedirect.com/science/article/pii/S1749461313000304},
doi = {http://dx.doi.org/10.1016/j.fbr.2013.05.003},
issn = {1749-4613},
year = {2013},
date = {2013-01-01},
journal = {Fungal Biology Reviews},
number = {0},
pages = {-},
abstract = {Abstract Label-free fluorescence microscopy detects fluorescence originating from endogenous fluorophores, such as NAD(P)H, melanin and flavins. The emitted fluorescence (spectrum, lifetime and polarization) is characteristic for the molecule and its environment. In most cases, a specimen contains multiple autofluorescent molecules contributing to the overall fluorescence. Methods have been developed to break down the fluorescence into the contribution of its individual components. As a result, label-free microscopy can map biochemical properties of fluorophores spatially and over time at the level of the organism, tissue and cells. This is of interest for fungal cell biology and development. Moreover, it can be used in biotechnological applications to monitor the metabolic state within a bioreactor or to monitor the formation of secondary metabolites. Combining morphological and biochemical properties can also lead to new developments in fungal taxonomy, biomedical diagnostics, as well as the screening of fungal products such as mushrooms.},
note = {in press},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
Karreman, Matthia A.; Buurmans, Inge L. C.; Agronskaia, Alexandra V.; Geus, John W.; Gerritsen, Hans C.; Weckhuysen, Bert M.
Probing the different life stages of a fluid catalytic cracking particle with integrated laser and electron microscopy Journal Article
In: Chemistry - A European Journal, vol. 19, no. 12, pp. 3846-3859, 2013, (cited By (since 1996) 0).
@article{Karreman20133846,
title = {Probing the different life stages of a fluid catalytic cracking particle with integrated laser and electron microscopy},
author = {Matthia A. Karreman and Inge L.C. Buurmans and Alexandra V. Agronskaia and John W. Geus and Hans C. Gerritsen and Bert M. Weckhuysen},
url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-84874956221&partnerID=40&md5=72b6f2ef1b89aa61bc7980e511ff7982},
year = {2013},
date = {2013-01-01},
journal = {Chemistry - A European Journal},
volume = {19},
number = {12},
pages = {3846-3859},
abstract = {While cycling through a fluid catalytic cracking (FCC) unit, the structure and performance of FCC catalyst particles are severely affected. In this study, we set out to characterize the damage to commercial equilibrium catalyst particles, further denoted as ECat samples, and map the different pathways involved in their deactivation in a practical unit. The degradation was studied on a structural and a functional level. Transmission electron microscopy (TEM) of ECat samples revealed several structural features; including zeolite crystals that were partly or fully severed, mesoporous, macroporous, and/or amorphous. These defects were then correlated to structural features observed in FCC particles that were treated with different levels of hydrothermal deactivation. This allowed us not only to identify which features observed in ECat samples were a result of hydrothermal deactivation, but also to determine the severity of treatments resulting in these defects. For functional characterization of the ECat sample, the Brønsted acidity within individual FCC particles was studied by a selective fluorescent probe reaction with 4-fluorostyrene. Integrated laser and electron microscopy (iLEM) allowed correlating this Brønsted acidity to structural features by combining a fluorescence and a transmission electron microscope in a single set-up. Together, these analyses allowed us to postulate a plausible model for the degradation of zeolite crystals in FCC particles in the ECat sample. Furthermore, the distribution of the various deactivation processes within particles of different ages was studied. A rim of completely deactivated zeolites surrounding each particle in the ECat sample was identified by using iLEM. These zeolites, which were never observed in fresh or steam-deactivated samples, contained clots of dense structures. The structures are proposed to be carbonaceous deposits formed during the cracking process, and seem resistant towards burning off during catalyst regeneration. Exposing the cracks: Several processes in an industrial fluid catalytic cracking (FCC) unit lead to deactivation of FCC particles. A structural and functional analysis of hydrothermally deactivated FCC particles and particles from a commercial equilibrium catalyst particle (ECat) sample was performed. A model is postulated for the degradation of the zeolite component. Inter- and intraparticle distributions of defects were mapped, resulting in the identification of a rim of fully deactivated zeolites (see figure). Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.},
note = {cited By (since 1996) 0},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
Faas, Frank G. A.; Bárcena, Montserrat; Agronskaia, Alexandra V.; Gerritsen, Hans C.; Moscicka, Katarzyna B.; Diebolder, Christoph A.; van Driel, Linda F.; Limpens, Ronald W. A. L.; Bos, Erik; Ravelli, Raimond B. G.; Koning, Roman I.; Koster, Abraham J.
Localization of fluorescently labeled structures in frozen-hydrated samples using integrated light electron microscopy Journal Article
In: Journal of Structural Biology, vol. 181, no. 3, pp. 283-290, 2013, (cited By (since 1996) 0).
@article{Faas2013283,
title = {Localization of fluorescently labeled structures in frozen-hydrated samples using integrated light electron microscopy},
author = {Frank G.A. Faas and Montserrat Bárcena and Alexandra V. Agronskaia and Hans C. Gerritsen and Katarzyna B. Moscicka and Christoph A. Diebolder and Linda F. van Driel and Ronald W.A.L. Limpens and Erik Bos and Raimond B.G. Ravelli and Roman I. Koning and Abraham J. Koster},
url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-84874000908&partnerID=40&md5=07de417233471010ab2ddb151974b31e},
year = {2013},
date = {2013-01-01},
journal = {Journal of Structural Biology},
volume = {181},
number = {3},
pages = {283-290},
abstract = {Correlative light and electron microscopy is an increasingly popular technique to study complex biological systems at various levels of resolution. Fluorescence microscopy can be employed to scan large areas to localize regions of interest which are then analyzed by electron microscopy to obtain morphological and structural information from a selected field of view at nm-scale resolution. Previously, an integrated approach to room temperature correlative microscopy was described. Combined use of light and electron microscopy within one instrument greatly simplifies sample handling, avoids cumbersome experimental overheads, simplifies navigation between the two modalities, and improves the success rate of image correlation. Here, an integrated approach for correlative microscopy under cryogenic conditions is presented. Its advantages over the room temperature approach include safeguarding the native hydrated state of the biological specimen, preservation of the fluorescence signal without risk of quenching due to heavy atom stains, and reduced photo bleaching. The potential of cryo integrated light and electron microscopy is demonstrated for the detection of viable bacteria, the study of in vitro polymerized microtubules, the localization of mitochondria in mouse embryonic fibroblasts, and for a search into virus-induced intracellular membrane modifications within mammalian cells. © 2012 Elsevier Inc.},
note = {cited By (since 1996) 0},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
van Spronsen, Myrrhe; Mikhaylova, Marina; Lipka, Joanna; Schlager, Max A.; van den Heuvel, Dave J.; Kuijpers, Marijn; Wulf, Phebe S.; Keijzer, Nanda; Demmers, Jeroen A. A.; Kapitein, Lukas C.; Jaarsma, Dick; Gerritsen, Hans C.; Akhmanova, Anna S.; Hoogenraad, Casper C.
TRAK/Milton Motor-Adaptor Proteins Steer Mitochondrial Trafficking to Axons and Dendrites Journal Article
In: Neuron, vol. 77, no. 3, pp. 485-502, 2013, (cited By (since 1996) 0).
@article{vanSpronsen2013485,
title = {TRAK/Milton Motor-Adaptor Proteins Steer Mitochondrial Trafficking to Axons and Dendrites},
author = {Myrrhe van Spronsen and Marina Mikhaylova and Joanna Lipka and Max A. Schlager and Dave J. van den Heuvel and Marijn Kuijpers and Phebe S. Wulf and Nanda Keijzer and Jeroen A.A. Demmers and Lukas C. Kapitein and Dick Jaarsma and Hans C. Gerritsen and Anna S. Akhmanova and Casper C. Hoogenraad},
url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-84873279659&partnerID=40&md5=53f917e82bb41c31d7cd3eaf1ebdb2b4},
year = {2013},
date = {2013-01-01},
journal = {Neuron},
volume = {77},
number = {3},
pages = {485-502},
abstract = {In neurons, the distinct molecular composition of axons and dendrites is established through polarized targeting mechanisms, but it is currently unclear how nonpolarized cargoes, such as mitochondria, become uniformly distributed over these specialized neuronal compartments. Here, we show that TRAK family adaptor proteins, TRAK1 and TRAK2, which link mitochondria to microtubule-based motors, are required for axonal and dendritic mitochondrial motility and utilize different transport machineries to steer mitochondria into axons and dendrites. TRAK1 binds to both kinesin-1 and dynein/dynactin, is prominently localized in axons, and is needed for normal axon outgrowth, whereas TRAK2 predominantly interacts with dynein/dynactin, is more abundantly present in dendrites, and is required for dendritic development. These functional differences follow from their distinct conformations: TRAK2 preferentially adopts a head-to-tail interaction, which interferes with kinesin-1 binding and axonal transport. Our study demonstrates how the molecular interplay between bidirectional adaptor proteins and distinct microtubule-based motors drives polarized mitochondrial transport. van Spronsen et al. show that mitochondria utilize different machineries to steer their transport into axons and dendrites. The molecular interplay between mitochondrial adaptor protein family TRAK/Milton and distinct microtubule-based motors drives polarized mitochondrial transport. © 2013 Elsevier Inc.},
note = {cited By (since 1996) 0},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
Knaus, Helene; Blab, Gerhard A.; Agronskaia, Alexandra V.; van den Heuvel, Dave J.; Gerritsen, Hans C.; Wösten, Han A. B.
Monitoring the metabolic state of fungal hyphae and the presence of melanin by nonlinear spectral imaging Journal Article
In: Applied and Environmental Microbiology, vol. 79, no. 20, pp. 6345-6350, 2013, (cited By 2).
@article{Knaus20136345,
title = {Monitoring the metabolic state of fungal hyphae and the presence of melanin by nonlinear spectral imaging},
author = {Helene Knaus and Gerhard A. Blab and Alexandra V. Agronskaia and Dave J. van den Heuvel and Hans C. Gerritsen and Han A.B. Wösten},
url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-84885037949&partnerID=40&md5=d7640036730e5e1be25a63231c0c47ec},
doi = {10.1128/AEM.02291-13},
year = {2013},
date = {2013-01-01},
journal = {Applied and Environmental Microbiology},
volume = {79},
number = {20},
pages = {6345-6350},
note = {cited By 2},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
Fereidouni, Farzad; Blab, Gerhard A.; Gerritsen, Hans C.
Blind unmixing of spectrally resolved lifetime images Journal Article
In: Journal of Biomedical Optics, vol. 18, no. 8, 2013, (cited By 6).
@article{Fereidouni2013,
title = {Blind unmixing of spectrally resolved lifetime images},
author = {Farzad Fereidouni and Gerhard A. Blab and Hans C. Gerritsen},
url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-84892490015&partnerID=40&md5=2a47200af50b1f0806307feacaca9673},
doi = {10.1117/1.JBO.18.8.086006},
year = {2013},
date = {2013-01-01},
journal = {Journal of Biomedical Optics},
volume = {18},
number = {8},
note = {cited By 6},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
2012
Nadiarnykh, Oleg; Thomas, Giju; van Voskuilen, Johan; Sterenborg, Henricus J. C. M.; Gerritsen, Hans C.
In: J Biomed Opt, vol. 17, no. 11, pp. 116024, 2012, ([PubMed:hrefhttp://www.ncbi.nlm.nih.gov/pubmed/2321418523214185]).
@article{pmid23214185,
title = {Carcinogenic damage to deoxyribonucleic acid is induced by near-infrared laser pulses in multiphoton microscopy via combination of two- and three-photon absorption},
author = {Oleg Nadiarnykh and Giju Thomas and Johan van Voskuilen and Henricus J.C.M. Sterenborg and Hans C. Gerritsen},
year = {2012},
date = {2012-11-01},
journal = {J Biomed Opt},
volume = {17},
number = {11},
pages = {116024},
abstract = {Nonlinear optical imaging modalities (multiphoton excited fluorescence, second and third harmonic generation) applied in vivo are increasingly promising for clinical diagnostics and the monitoring of cancer and other disorders, as they can probe tissue with high diffraction-limited resolution at near-infrared (IR) wavelengths. However, high peak intensity of femtosecond laser pulses required for two-photon processes causes formation of cyclobutane-pyrimidine-dimers (CPDs) in cellular deoxyribonucleic acid (DNA) similar to damage from exposure to solar ultraviolet (UV) light. Inaccurate repair of subsequent mutations increases the risk of carcinogenesis. In this study, we investigate CPD damage that results in Chinese hamster ovary cells in vitro from imaging them with two-photon excited autofluorescence. The CPD levels are quantified by immunofluorescent staining. We further evaluate the extent of CPD damage with respect to varied wavelength, pulse width at focal plane, and pixel dwell time as compared with more pronounced damage from UV sources. While CPD damage has been expected to result from three-photon absorption, our results reveal that CPDs are induced by competing twoand three-photon absorption processes, where the former accesses UVA absorption band. This finding is independently confirmed by nonlinear dependencies of damage on laser power, wavelength, and pulse width.},
note = {[PubMed:hrefhttp://www.ncbi.nlm.nih.gov/pubmed/2321418523214185]},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
Gitz, Eelo; Koekman, Cornelis A.; van den Heuvel, Dave J.; Deckmyn, Hans; Akkerman, Jan Willem N.; Gerritsen, Hans C.; Urbanus, Rolf T.
Improved platelet survival after cold storage by prevention of glycoprotein Ibα clustering in lipid rafts Journal Article
In: Haematologica, vol. 97, no. 12, pp. 1873-1881, 2012, (cited By (since 1996) 1).
@article{Gitz20121873,
title = {Improved platelet survival after cold storage by prevention of glycoprotein Ibα clustering in lipid rafts},
author = {Eelo Gitz and Cornelis A. Koekman and Dave J. van den Heuvel and Hans Deckmyn and Jan Willem N. Akkerman and Hans C. Gerritsen and Rolf T. Urbanus},
url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-84869885949&partnerID=40&md5=446f25fb0e7209b3093c1006feeb7767},
year = {2012},
date = {2012-01-01},
journal = {Haematologica},
volume = {97},
number = {12},
pages = {1873-1881},
abstract = {Background Storing platelets for transfusion at room temperature increases the risk of microbial infection and decreases platelet functionality, leading to out-date discard rates of up to 20%. Cold storage may be a better alternative, but this treatment leads to rapid platelet clearance after transfusion, initiated by changes in glycoprotein Ibα, the receptor for von Willebrand factor. Design and Methods We examined the change in glycoprotein Ibα distribution using Förster resonance energy transfer by time-gated fluorescence lifetime imaging microscopy. Results Cold storage induced deglycosylation of glycoprotein Ibα ectodomain, exposing N-acetyl-D-glucosamine residues, which sequestered with GM1 gangliosides in lipid rafts. Raft-associated glycoprotein Ibα formed clusters upon binding of 14-3-3ζ adaptor proteins to its cytoplasmic tail, a process accompanied by mitochondrial injury and phosphatidyl serine exposure. Cold storage left glycoprotein Ibα surface expression unchanged and although glycoprotein V decreased, the fall did not affect glycoprotein Ibα clustering. Prevention of glycoprotein Ibα clustering by blockade of deglycosylation and 14-3-3ζ translocation increased the survival of cold-stored platelets to above the levels of platelets stored at room temperature without compromising hemostatic functions. Conclusions We conclude that glycoprotein Ibα translocates to lipid rafts upon cold-induced deglycosylation and forms clusters by associating with 14-3-3ζ. Interference with these steps provides a means to enable cold storage of platelet concentrates in the near future. © 2012 Ferrata Storti Foundation.},
note = {cited By (since 1996) 1},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
Antonello, Jacopo; Verhaegen, Michel H. G.; Fraanje, Rufus; van Werkhoven, Tim; Gerritsen, Hans C.; Keller, Christoph U.
Semidefinite programming for model-based sensorless adaptive optics Journal Article
In: Journal of the Optical Society of America A: Optics and Image Science, and Vision, vol. 29, no. 11, pp. 2428-2438, 2012, (cited By (since 1996) 0).
@article{Antonello20122428,
title = {Semidefinite programming for model-based sensorless adaptive optics},
author = {Jacopo Antonello and Michel H.G. Verhaegen and Rufus Fraanje and Tim van Werkhoven and Hans C. Gerritsen and Christoph U. Keller},
url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-84869786716&partnerID=40&md5=202137cf58ed5b14c167285f48295edc},
year = {2012},
date = {2012-01-01},
journal = {Journal of the Optical Society of America A: Optics and Image Science, and Vision},
volume = {29},
number = {11},
pages = {2428-2438},
abstract = {Wavefront sensorless adaptive optics methodologies are widely considered in scanning fluorescence microscopy where direct wavefront sensing is challenging. In these methodologies, aberration correction is performed by sequentially changing the settings of the adaptive element until a predetermined image quality metric is optimized. An efficient aberration correction can be achieved by modeling the image quality metric with a quadratic polynomial. We propose a new method to compute the parameters of the polynomial from experimental data. This method guarantees that the quadratic form in the polynomial is semidefinite, resulting in a more robust computation of the parameters with respect to existing methods. In addition, we propose an algorithm to perform aberration correction requiring a minimum of N + 1 measurements, where N is the number of considered aberration modes. This algorithm is based on a closed-form expression for the exact optimization of the quadratic polynomial. Our arguments are corroborated by experimental validation in a laboratory environment. © 2012 Optical Society of America.},
note = {cited By (since 1996) 0},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
Karreman, Matthia A.; Agronskaia, Alexandra V.; van Donselaar, Elly G.; Vocking, Karin; Fereidouni, Farzad; Humbel, Bruno M.; Verrips, Cornelis T.; Verkleij, Ariel J.; Gerritsen, Hans C.
Optimizing immuno-labeling for correlative fluorescence and electron microscopy on a single specimen Journal Article
In: Journal of Structural Biology, vol. 180, no. 2, pp. 382-386, 2012, (cited By (since 1996) 1).
@article{Karreman2012382,
title = {Optimizing immuno-labeling for correlative fluorescence and electron microscopy on a single specimen},
author = {Matthia A. Karreman and Alexandra V. Agronskaia and Elly G. van Donselaar and Karin Vocking and Farzad Fereidouni and Bruno M. Humbel and Cornelis T. Verrips and Ariel J. Verkleij and Hans C. Gerritsen},
url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-84867908573&partnerID=40&md5=b6914e9a5caa2dc078389ca3daf42596},
year = {2012},
date = {2012-01-01},
journal = {Journal of Structural Biology},
volume = {180},
number = {2},
pages = {382-386},
abstract = {Correlative fluorescence and electron microscopy has become an indispensible tool for research in cell biology. The integrated Laser and Electron Microscope (iLEM) combines a Fluorescence Microscope (FM) and a Transmission Electron Microscope (TEM) within one set-up. This unique imaging tool allows for rapid identification of a region of interest with the FM, and subsequent high resolution TEM imaging of this area. Sample preparation is one of the major challenges in correlative microscopy of a single specimen; it needs to be apt for both FM and TEM imaging. For iLEM, the performance of the fluorescent probe should not be impaired by the vacuum of the TEM. In this technical note, we have compared the fluorescence intensity of six fluorescent probes in a dry, oxygen free environment relative to their performance in water. We demonstrate that the intensity of some fluorophores is strongly influenced by its surroundings, which should be taken into account in the design of the experiment. Furthermore, a freeze-substitution and Lowicryl resin embedding protocol is described that yields excellent membrane contrast in the TEM but prevents quenching of the fluorescent immuno-labeling. The embedding protocol results in a single specimen preparation procedure that performs well in both FM and TEM. Such procedures are not only essential for the iLEM, but also of great value to other correlative microscopy approaches. © 2012 Elsevier Inc.},
note = {cited By (since 1996) 1},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
Nadiarnykh, Oleg; GijuThomas,; van Voskuilen, Johan; Sterenborg, Henricus J. C. M.; Gerritsen, Hans C.
In: Journal of Biomedical Optics, vol. 17, no. 11, 2012, (cited By (since 1996) 0).
@article{Nadiarnykh2012,
title = {Carcinogenic damage to deoxyribonucleic acid is induced by near-infrared laser pulses in multiphoton microscopy via combination of two- and three-photon absorption},
author = {Oleg Nadiarnykh and GijuThomas and Johan van Voskuilen and Henricus J.C.M. Sterenborg and Hans C. Gerritsen},
url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-84870600800&partnerID=40&md5=f65f5c42391abae69f91aa4b7a8939b8},
year = {2012},
date = {2012-01-01},
journal = {Journal of Biomedical Optics},
volume = {17},
number = {11},
abstract = {Nonlinear optical imaging modalities (multiphoton excited fluorescence, second and third harmonic generation) applied in vivo are increasingly promising for clinical diagnostics and the monitoring of cancer and other disorders, as they can probe tissue with high diffraction-limited resolution at near-infrared (IR) wavelengths. However, high peak intensity of femtosecond laser pulses required for two-photon processes causes formation of cyclobutane-pyrimidine- dimers (CPDs) in cellular deoxyribonucleic acid (DNA) similar to damage from exposure to solar ultraviolet (UV) light. Inaccurate repair of subsequent mutations increases the risk of carcinogenesis. In this study, we investigate CPD damage that results in Chinese hamster ovary cells in vitro from imaging them with two-photon excited autofluorescence. The CPD levels are quantified by immunofluorescent staining. We further evaluate the extent of CPD damage with respect to varied wavelength, pulse width at focal plane, and pixel dwell time as compared with more pronounced damage from UV sources. While CPD damage has been expected to result from three-photon absorption, our results reveal that CPDs are induced by competing twoand three-photon absorption processes, where the former accesses UVA absorption band. This finding is independently confirmed by nonlinear dependencies of damage on laser power, wavelength, and pulse width. © 2012 Society of Photo-Optical Instrumentation Engineers (SPIE).},
note = {cited By (since 1996) 0},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
Hafrén, Jonas; Nelsson, Erik; Gerritsen, Hans C.; Bader, Arjen N.
In: Holzforschung, vol. 66, no. 7, pp. 817-824, 2012, (cited By (since 1996) 0).
@article{Hafrén2012817,
title = {Optical properties of thermomechanical pulp (TMP) obtained from sulfite-pretreated Norway spruce with focus on two-photon spectral imaging (TPSI)},
author = {Jonas Hafrén and Erik Nelsson and Hans C. Gerritsen and Arjen N. Bader},
url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-84869416158&partnerID=40&md5=788802190d7fc7d0b9af3dd9e425b8d3},
year = {2012},
date = {2012-01-01},
journal = {Holzforschung},
volume = {66},
number = {7},
pages = {817-824},
abstract = {Chips of Norway spruce have been impregnated with Na2SO 3 and refined at two specific energy consumptions levels at full mill scale. The optical properties of thermomechanical pulps (TMPs) obtained were analyzed in terms of brightness, light scattering, opacity, and autofluorescence by spectral imaging. Even at low sulfite dosage (0.24% sulfite by dry weight) light absorption was reduced, and the brightness was elevated, and a clear dose-response effect was observed. Two-photon spectral imaging (TPSI) showed that sulfonation, impregnation, and refining affect the fluorescence properties differently. Compared to native wood, both processed wood chips and pulp fibers revealed blue-shifted fluorescence maxima, a characteristic of shortened conjugated systems. Two subpopulations of fibers with different optical properties were observed, and the fluorescence of one fiber population was red shifted. Copyright © by Walter de Gruyter.},
note = {cited By (since 1996) 0},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
Antonello, Jacopo; Fraanje, Rufus; Song, Hong; Verhaegen, Michel H. G.; Gerritsen, Hans C.; Keller, Christoph U.; van Werkhoven, Tim
Data driven identification and aberration correction for model based sensorless adaptive optics Conference
vol. 8436, 2012, (cited By (since 1996) 1).
@conference{Antonello2012,
title = {Data driven identification and aberration correction for model based sensorless adaptive optics},
author = {Jacopo Antonello and Rufus Fraanje and Hong Song and Michel H.G. Verhaegen and Hans C. Gerritsen and Christoph U. Keller and Tim van Werkhoven},
url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-84861929346&partnerID=40&md5=48c56c6ae5a0b37bfdaa2aa70fe8274c},
year = {2012},
date = {2012-01-01},
journal = {Proceedings of SPIE - The International Society for Optical Engineering},
volume = {8436},
abstract = {Wavefront sensorless adaptive optics methodologies are considered in many applications where the deployment of a dedicated wavefront sensor is inconvenient, such as in fluorescence microscopy. In these methodologies, aberration correction is achieved by sequentially changing the settings of the adaptive optical element until a predetermined imaging quality metric is optimised. Reducing the time required for this optimisation is a challenge. In this paper, a two stage data driven optimisation procedure is presented and validated in a laboratory environment. In the first stage, known aberrations are introduced by a deformable mirror and the corresponding intensities are measured by a photodiode masked by a pinhole. A generic quadratic metric is fitted to this collection of aberrations and intensity measurements. In the second stage, this quadratic metric is used in order to estimate and correct for optical aberrations. A closed form expression for the optimisation of the quadratic metric is derived by solving a linear system of equations. This requires a minimum of N +1 pairs of deformable mirror settings and intensity measurements, where N is the number of modes of the aberrations. © 2012 SPIE.},
note = {cited By (since 1996) 1},
keywords = {},
pubstate = {published},
tppubtype = {conference}
}
Fereidouni, Farzad; Bader, Arjen N.; Gerritsen, Hans C.
Spectral phasor analysis allows rapid and reliable unmixing of fluorescence microscopy spectral images Journal Article
In: Optics Express, vol. 20, no. 12, pp. 12729-12741, 2012, (cited By (since 1996) 1).
@article{Fereidouni201212729,
title = {Spectral phasor analysis allows rapid and reliable unmixing of fluorescence microscopy spectral images},
author = {Farzad Fereidouni and Arjen N. Bader and Hans C. Gerritsen},
url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-84863773951&partnerID=40&md5=d006a9341028995b35df3c3e49d740eb},
year = {2012},
date = {2012-01-01},
journal = {Optics Express},
volume = {20},
number = {12},
pages = {12729-12741},
abstract = {A new global analysis algorithm to analyse (hyper-) spectral images is presented. It is based on the phasor representation that has been demonstrated to be very powerful for the analysis of lifetime imaging data. In spectral phasor analysis the fluorescence spectrum of each pixel in the image is Fourier transformed. Next, the real and imaginary components of the first harmonic of the transform are employed as X and Y coordinates in a scatter (spectral phasor) plot. Importantly, the spectral phasor representation allows for rapid (real time) semi-blind spectral unmixing of up to three components in the image. This is demonstrated on slides with fixed cells containing three fluorescent labels. In addition the method is used to analyse autofluorescence of cells in a fresh grass blade. It is shown that the spectral phasor approach is compatible with spectral imaging data recorded with a low number of spectral channels. ©2012 Optical Society of America.},
note = {cited By (since 1996) 1},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
van Werkhoven, Tim; Truong, Hoa H.; Antonello, Jacopo; Fraanje, Rufus; Gerritsen, Hans C.; Verhagen, Michel H. G.; Keller, Christoph U.
Coherence-gated wavefront sensing for microscopy using fringe analysis Conference
vol. 8253, 2012, (cited By (since 1996) 0).
@conference{VanWerkhoven2012,
title = {Coherence-gated wavefront sensing for microscopy using fringe analysis},
author = {Tim van Werkhoven and Hoa H. Truong and Jacopo Antonello and Rufus Fraanje and Hans C. Gerritsen and Michel H.G. Verhagen and Christoph U. Keller},
url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-84859575448&partnerID=40&md5=e916490497126bed67217780e89f9f12},
year = {2012},
date = {2012-01-01},
journal = {Proceedings of SPIE - The International Society for Optical Engineering},
volume = {8253},
abstract = {We have implemented a coherence-gated wavefront sensor on a two-photon excitation microscope. We used the backscattered near-infrared light from the sample to interfere with an optically flat reference beam. By applying a known wavefront tilt in the reference beam, a fringe pattern emerged on the camera. The deformation of the wavefront due to the turbid media under study warps the fringe pattern, similar to frequency modulation. Through Fourier transform analysis of the modulated fringe pattern we were able to determine the wavefront aberrations induced by synthetic and biological samples. By defocussing the microscope objective and measuring the wavefront deformation we established that the errors are reproducible to within λ/227 for the defocus mode. © 2012 SPIE.},
note = {cited By (since 1996) 0},
keywords = {},
pubstate = {published},
tppubtype = {conference}
}
Groeneveld, Esther; van Berkum, Susanne; van Schooneveld, Matti M.; Gloter, Alexandre; Meeldijk, Johannes D.; van den Heuvel, Dave J.; Gerritsen, Hans C.; de Mello-Donega, Celso
Highly luminescent (Zn,Cd)Te/CdSe colloidal heteronanowires with tunable electron-hole overlap Journal Article
In: Nano Letters, vol. 12, no. 2, pp. 749-757, 2012, (cited By (since 1996) 6).
@article{Groeneveld2012749,
title = {Highly luminescent (Zn,Cd)Te/CdSe colloidal heteronanowires with tunable electron-hole overlap},
author = {Esther Groeneveld and Susanne van Berkum and Matti M. van Schooneveld and Alexandre Gloter and Johannes D. Meeldijk and Dave J. van den Heuvel and Hans C. Gerritsen and Celso de Mello-Donega},
url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-84856966346&partnerID=40&md5=9e3e8969e44eb2805065f4733e934adf},
year = {2012},
date = {2012-01-01},
journal = {Nano Letters},
volume = {12},
number = {2},
pages = {749-757},
abstract = {We report the synthesis of ultranarrow (Zn,Cd)Te/CdSe colloidal heteronanowires, using ZnTe magic size clusters as seeds. The wire formation starts with a partial Zn for Cd cation exchange, followed by self-organization into segmented heteronanowires. Further growth occurs by inclusion of CdSe. The heteronanowires emit in the 530 to 760 nm range with high quantum yields. The electron-hole overlap decreases with increasing CdSe volume fraction, allowing the optical properties to be controlled by adjusting the heteronanowire composition. © 2012 American Chemical Society.},
note = {cited By (since 1996) 6},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
Karreman, Matthia A.; Buurmans, Inge L. C.; Geus, John W.; Agronskaia, Alexandra V.; Ruiz-Martínez, Javier; Gerritsen, Hans C.; Weckhuysen, Bert M.
Integrated laser and electron microscopy correlates structure of fluid catalytic cracking particles to Brønsted acidity Journal Article
In: Angewandte Chemie - International Edition, vol. 51, no. 6, pp. 1428-1431, 2012, (cited By (since 1996) 5).
@article{Karreman20121428,
title = {Integrated laser and electron microscopy correlates structure of fluid catalytic cracking particles to Brønsted acidity},
author = {Matthia A. Karreman and Inge L.C. Buurmans and John W. Geus and Alexandra V. Agronskaia and Javier Ruiz-Martínez and Hans C. Gerritsen and Bert M. Weckhuysen},
url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-84856448244&partnerID=40&md5=48a205b66e1adb856ca1c10359c379ce},
year = {2012},
date = {2012-01-01},
journal = {Angewandte Chemie - International Edition},
volume = {51},
number = {6},
pages = {1428-1431},
abstract = {Cracking the crackers: Integrated laser and electron microscopy was applied to study individual fluid catalytic cracking catalyst particles (see picture) deactivated according to an industrially relevant protocol. New insights have been obtained by correlating Brønsted acidity changes, visualized using fluorescence microscopy, with structural transformations in the zeolite and matrix components, as observed with electron microscopy. Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.},
note = {cited By (since 1996) 5},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
Kovacic, Suzana; Samii, Laleh; Woolfson, Dek N.; Curmi, Paul M. G.; Linke, Heiner; Forde, Nancy R.; Blab, Gerhard A.
Design and construction of a one-dimensional DNA track for an artificial molecular motor Journal Article
In: Journal of Nanomaterials, vol. 2012, 2012, ISSN: 16874110.
@article{Kovacic2012,
title = {Design and construction of a one-dimensional DNA track for an artificial molecular motor},
author = {Suzana Kovacic and Laleh Samii and Dek N. Woolfson and Paul M.G. Curmi and Heiner Linke and Nancy R. Forde and Gerhard A. Blab},
url = {http://www.hindawi.com/journals/jnm/2012/109238/},
doi = {10.1155/2012/109238},
issn = {16874110},
year = {2012},
date = {2012-01-01},
journal = {Journal of Nanomaterials},
volume = {2012},
abstract = {DNA is a versatile heteropolymer that shows great potential as a building block for a diverse array of nanostructures. We present here a solution to the problem of designing and synthesizing a DNA-based nanostructure that will serve as the track along which an artificial molecular motor processes. This one-dimensional DNA track exhibits periodically repeating elements that provide specific binding sites for the molecular motor. Besides these binding elements, additional sequences are necessary to label specific regions within the DNA track and to facilitate track construction. Designing an ideal DNA track sequence presents a particular challenge because of the many variable elements that greatly expand the number of potential sequences from which the ideal sequence must be chosen. In order to find a suitable DNA sequence, we have adapted a genetic algorithm which is well suited for a large but sparse search space. This algorithm readily identifies long DNA sequences that include all the necessary elements to both facilitate DNA track construction and to present appropriate binding sites for the molecular motor. We have successfully experimentally incorporated the sequence identified by the algorithm into a long DNA track meeting the criteria for observation of the molecular motor's activity. © 2012 Suzana Kovacic et al.},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
2011
Fereidouni, Farzad; Esposito, Alessandro; Blab, Gerhard A.; Gerritsen, Hans C.
A modified phasor approach for analyzing time-gated fluorescence lifetime images Journal Article
In: Journal of Microscopy, vol. 244, no. 3, pp. 248-258, 2011, (cited By (since 1996) 4).
@article{Fereidouni2011248,
title = {A modified phasor approach for analyzing time-gated fluorescence lifetime images},
author = {Farzad Fereidouni and Alessandro Esposito and Gerhard A. Blab and Hans C. Gerritsen},
url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-81255168136&partnerID=40&md5=8c5891d4a795370fea469dc374564281},
year = {2011},
date = {2011-01-01},
journal = {Journal of Microscopy},
volume = {244},
number = {3},
pages = {248-258},
abstract = {Fluorescence lifetime imaging is a versatile tool that permits mapping the biochemical environment in the cell. Among various fluorescence lifetime imaging techniques, time-correlated single photon counting and time-gating methods have been demonstrated to be very efficient and robust for the imaging of biological specimens. Recently, the phasor representation of lifetime images became popular because it provides an intuitive graphical view of the fluorescence lifetime content of the images and, when used for global analysis, significantly improves the overall S/N of lifetime analysis. Compared to time-correlated single photon counting, time gating methods can provide higher count rates (∼10 MHz) but at the cost of truncating and under sampling the decay curve due to the limited number of gates commonly used. These limitations also complicate the implementation of the phasor analysis for time-gated data. In this work, we propose and validate a theoretical framework that overcomes these problems. This modified approach is tested on both simulated lifetime images and on cells. We demonstrate that this method is able to retrieve two lifetimes from time gating data that cannot be resolved using standard (non-global) fitting techniques. The new approach increases the information that can be obtained from typical measurements and simplifies the analysis of fluorescence lifetime imaging data. © 2011 Utrecht University Journal of Microscopy © 2011 Royal Microscopical Society.},
note = {cited By (since 1996) 4},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
Hafrén, Jonas; Muhić, Dino; Gerritsen, Hans C.; Bader, Arjen N.
Two-photon autofluorescence spectral imaging applied to probe process-effects in thermomechanical pulp refining Journal Article
In: Nordic Pulp and Paper Research Journal, vol. 26, no. 4, pp. 372-379, 2011, (cited By (since 1996) 2).
@article{Hafrén2011372,
title = {Two-photon autofluorescence spectral imaging applied to probe process-effects in thermomechanical pulp refining},
author = {Jonas Hafrén and Dino Muhić and Hans C. Gerritsen and Arjen N. Bader},
url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-84855522085&partnerID=40&md5=36170ed2f702bc3a5d28fb0ce8eed179},
year = {2011},
date = {2011-01-01},
journal = {Nordic Pulp and Paper Research Journal},
volume = {26},
number = {4},
pages = {372-379},
abstract = {Norway spruce wood pulps were produced in full industrial scale trials at different thermomechanical pulp refining conditions, such as plate gap, housing pressures and energy consumption levels. To investigate the effects of these refining conditions on the lingocellulosic matrix in fines and fibers, we applied high-resolution spectral imaging in a two-photon fluorescence microscope and compared with conventional pulp and paper analyses (strength, freeness etc.). The fluorescence spectra of lignin in native wood and fibersand fines from pulps showed that spatial- and spectral heterogeneities can be observed using two-photon autofluorescence spectral imaging, and successfully probed on a microscopic level. Moreover, it was shown that wood autofluorescence depends on fiber morphology and becomes red-shifted by increased temperature, but the fluorescence spectrum of TMP long fiber fraction shifted towards blue by increased refining pressure.},
note = {cited By (since 1996) 2},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
van der Poel, Seléne; Wolthoorn, Jasja; van den Heuvel, Dave J.; Egmond, Maarten R.; Groux-Degroote, Sophie; Neumann, Sylvia; Gerritsen, Hans C.; van Meer, Gerrit; Sprong, Hein
Hyperacidification of trans-golgi network and endo/lysosomes in melanocytes by glucosylceramide-dependent V-ATPase activity Journal Article
In: Traffic, vol. 12, no. 11, pp. 1634-1647, 2011, (cited By (since 1996) 3).
@article{vanderPoel20111634,
title = {Hyperacidification of trans-golgi network and endo/lysosomes in melanocytes by glucosylceramide-dependent V-ATPase activity},
author = {Seléne van der Poel and Jasja Wolthoorn and Dave J. van den Heuvel and Maarten R. Egmond and Sophie Groux-Degroote and Sylvia Neumann and Hans C. Gerritsen and Gerrit van Meer and Hein Sprong},
url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-80053594845&partnerID=40&md5=15d915d33f87d797725c167358e89204},
year = {2011},
date = {2011-01-01},
journal = {Traffic},
volume = {12},
number = {11},
pages = {1634-1647},
abstract = {Sphingolipids are considered to play a key role in protein sorting and membrane trafficking. In melanocytic cells, sorting of lysosomal and melanosomal proteins requires the sphingolipid glucosylceramide (GlcCer). This sorting information is located in the lumenal domain of melanosomal proteins. We found that two processes dependent on lumenal pH, protein sialylation and lysosomal acid lipase (LAL) activity were aberrant in GM95 melanocyte cells, which do not produce glycosphingolipids. Using fluorescence lifetime imaging microscopy (FLIM), we found that the lumenal pH in the trans-Golgi network and lysosomes of wild-type melanocyte MEB4 cells are >1 pH unit lower than GM95 cells and fibroblasts. In addition to the lower pH found in vivo, the in vitro activity of the proton pump, the vacuolar-type H +-translocating ATPase (V-ATPase), was twofold higher in MEB4 compared to GM95 cells. The apparent K i for inhibition of the V-ATPase by concanamycin A and archazolid A, which share a common binding site on the c-ring, was lower in glycosphingolipid-deficient GM95 cells. No difference between the MEB4 and GM95 cells was found for the V-ATPase inhibitors apicularen A and salicylihalimide. We conclude that hyperacidification in MEB4 cells requires glycosphingolipids and propose that low pH is necessary for protein sorting and melanosome biogenesis. Furthermore, we suggest that glycosphingolipids are indirectly involved in protein sorting and melanosome biogenesis by stimulating the proton pump, possibly through binding of GlcCer. These experiments establish, for the first time, a link between pH, glycosphingolipids and melanosome biogenesis in melanocytic MEB4 cells, to suggest a role for glycosphingolipids in hyperacidification in melanocytes. © 2011 John Wiley & Sons A/S.},
note = {cited By (since 1996) 3},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
Elstak, Edo D.; Neeft, Maaike; Nehme, Nadine T.; Voortman, Jarno; Cheung, Marc; Goodarzifard, Monireh; Gerritsen, Hans C.; van Bergen en Henegouwen, Paul M. P.; Callebaut, Isabelle; de Saint Basile, Geneviève; van der Sluijs, Peter D.
The munc13-4-rab27 complex is specifically required for tethering secretory lysosomes at the plasma membrane Journal Article
In: Blood, vol. 118, no. 6, pp. 1570-1578, 2011, (cited By (since 1996) 12).
@article{Elstak20111570,
title = {The munc13-4-rab27 complex is specifically required for tethering secretory lysosomes at the plasma membrane},
author = {Edo D. Elstak and Maaike Neeft and Nadine T. Nehme and Jarno Voortman and Marc Cheung and Monireh Goodarzifard and Hans C. Gerritsen and Paul M.P. van Bergen en Henegouwen and Isabelle Callebaut and Geneviève de Saint Basile and Peter D. van der Sluijs},
url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-80051639052&partnerID=40&md5=4369791a6d23655b138e96021245dbfc},
year = {2011},
date = {2011-01-01},
journal = {Blood},
volume = {118},
number = {6},
pages = {1570-1578},
abstract = {Cytotoxic T lymphocytes (CTLs) kill target cells through the polarized release of lytic molecules from secretory lysosomes. Loss of munc13-4 function inhibits this process and causes familial hemophagocytic lymphohistiocytosis type 3 (FHL3). munc13-4 binds rab27a, but the necessity of the complex remains enigmatic, because studies in knockout models suggest separate functions. In the present study, we describe a noncanonical rab27abinding motif in the N-terminus of munc13-4. Point mutants in this sequence have severely impaired rab27a binding, allowing dissection of rab27a requirements in munc13-4 function. The munc13- 4 - rab27a complex is not needed for secretory lysosome maturation, as shown by complementation in CTLs from FHL3 patients and in a mast cell line silenced for munc13-4. In contrast, fusion of secretory lysosomes with, and content release at the plasma membrane during degranulation, strictly required the munc13-4 - rab27a complex. Total internal reflection fluorescence microscopy imaging revealed that the complex corrals motile secretory lysosomes beneath the plasma membrane during degranulation and controls their docking. The propensity to stall motility of secretory lysosomes is lost in cells expressing munc13-4 point mutants that do not bind rab27. In summary, these results uncovered a mechanism for tethering secretory lysosomes to the plasma membrane that is essential for degranulation in immune cells. © 2011 by The American Society of Hematology.},
note = {cited By (since 1996) 12},
keywords = {},
pubstate = {published},
tppubtype = {article}
}