Winners Huygens Image Contest
2023 Winners
- 1st Prize: Dr. Juraj Kabat, Biological Imaging Facility, NIAID/NIH, Bethesda, MD, USA
- 2nd Prize: Dr. Stéphanie Durand, Department of Chromosome Biology, Max Planck Institute for Plant Breeding Research, Cologne, Germany.
- 3rd Prize: Dr. Tatiana Alfonso-Pérez, Centro de Biología Molecular Severo Ochoa (CBMSO), Madrid, Spain.
- 4th Prize: Alexia Martin (PhD student) and Ellie Sweeney (Master's student) from Dr. Jorge Bernardino de la Serna's lab at Imperial College London and Professor Andrew Tutt's lab at the Institute of Cancer Research, UK.
- 5th Prize: Dr. Ioannis Alexopoulos, ILH/CIGL Multiscale Imaging Platform, Justus Liebig University Giessen, Germany
- 6th Prize: Dr. Vishakha Vishwakarma, Biological Sciences, Louisiana State University, Baton Rouge, LA, USA.
1st Prize Winner
Image from Juraj Kabat
Various Huygens options were used to produce this high quality and artistic picture. Mouse hair follicle visualized with the Huygens SFP renderer. Green is epithelial cells, Red is blood vessels, Cyan is lymphatic vessels, Magenta is CD45. Image was acquired on Leica Stellaris WLL system/confocal and opened in Huygens and corrected for unwanted movement (Object Stabilizer) and crosstalk, deconvolved, corrected for chromatic aberration, and visualized using Huygens SFP renderer.
2nd Prize Winner
Image from Stéphanie Durand
This picture stands out because of the high quality of microscopy and processing, showing a Maximum intensity projection of Huygens deconvolved STED image of a meiotic cell of Arabidopsis thaliana. Immuno-localization (green) of ZYP1, which forms the synaptonemal complex, a structure that zips the pair of homologous chromosomes all along their length at meiosis. ZYP1 is organized in a head-to-head configuration, with the C-ter end of the proteins on both sides, connected to the two homologous chromosomes. As the antibody recognizes the C-ter of ZYP1, the signals appear in super-resolution as two parallel lines distant by 78nm, corresponding to the pair of chromosomes.
3rd Prize Winner
Image from Tatiana Alfonso-Pérez
High quality data showing a Human cell in metaphase. During this stage of cell division, condensed chromosomes line up at the metaphase plate and attach to the mitotic spindle, a diamond-shape structure made up of microtubules and associated proteins. Left image was acquired using a Zeiss LSM800 confocal with 63X/1.4 objective. After acquisition, it was deconvolved with Huygens software (middle image), and rendered with Huygens Surface Renderer (right image). Left and middle images show DNA in blue, microtubules in red, and associated proteins in yellow. Right image shows microtubules in blue and associated proteins in green and red. This image was created with help of Mrs. Carmen Sanchez Jimenez from the Microscopy facility
4th Prize Winner
Image from Alexia Martin and Ellie Sweeney
Challenging imaging and image processing. This is a Huygens maximum intensity projection of a short extract of a 4D time lapse of live 3D MCF10A spheroids, with multiple cells in different stages of mitosis, imaged on a Leica Stellaris 5 Digital Light Sheet. Live staining of the DNA (green), microtubules (blue) and lipid membrane (red) in the spheroid can be seen in high resolution in a 3D volume. This imaging technique allows us to quantify and track mitotic segregation errors and chromosomal instability features for the identification of predictive biomarkers for anti-mitotic chemotherapies. Fusion, deconvolution, and rendering of multi-view spatiotemporal light sheet data is completed with Huygens software.
5th Prize Winner
Image from Ioannis Alexopoulos
Beautiful imaging. processing, and selection of LUT colors. Second Harmonic Generation and auto-fluorescence from histology, H&E stained, samples. Images were acquired with a Leica Dive 2photon system (10x/0.4NA air objective) using a Spectra Physics Insight X3+ laser tuned at 920nm. Upon acquisition and stiching, the images were deconvolved using the Deconvolution Express of Huygens Professional. Image represents a transverse cross section of a mouse tongue with the dorsal (upwards) and ventral part. At the dorsal surface the filiform papillae (small extensions in blue) are visible with auto-fluorescence collected at 470-540nm (blue labeled) and at 560-650nm (green labeled). Below that layer we can see the epithelium (multicellular layer with minimum auto-fluorescence), followed by collagen fibers (SHG in red). Then a thick layer of transverse and vertical muscle fibers follows. The myosin of the vertical muscle fibers is shown in magenta as the overlay of SHG and the blue-labeled auto-fluorescence. Scale bar 100um.
6th Prize Winner
Image from Vishakha Vishwakarma
Clear visualization of interesting phenotype. Unlike wild-type embryo (top panels), loss of Smog GPCR (bottom panels) results in slight disruption of the overall embryonic morphology, including defects in the head region, elongated salivary gland placode, a wavy embryo surface and an irregular ventral midline. 3D reconstructed images (middle panels) show the salivary gland placode elongated along the DV axis and enlarged cells upon loss of smog. Strikingly, smog loss also results in the formation of numerous blebs in the apical membrane of salivary gland cells, which are not observed in wild-type salivary gland cells, suggesting defects in the cortical actin network (rightmost panels). Overall, our work suggests multifunctional roles of GPCR signaling during epithelial morphogenesis.
2022 Winners
- 1st Prize: Dr. Ioannis Alexopoulos, ILH/CIGL Multiscale Imaging Platform, Justus Liebig University Giessen, Germany
- 2nd Prize: Blake Hernandez (PhD Student), Plachta Lab, Dept. of CDB, Perelman School of Medicine, University of Pennsylvania, USA
- 3rd Prize: Maaike Lambers (PhD Student), Kops group, Oncode Institute, Hubrecht Institute-KNAW, The Netherlands
- 4th Prize: Dr. Rolando Berlinguer Palmini, BioImaging Unit, Newcastle University, UK
- 5th Prize: Dr. Christian Jüngst, Imaging facility, CECAD Research Center, University of Cologne, Germany
1st Prize Winner
Image from Ioannis Alexopoulos
Movie of a 2-Photon tile scan of 40-days-old lung organoid, co-cultured with endothelial cells (green). The blue colour represents the DAPI nuclear marker and the orange the beta-Catenin. Sample prepared by Anna-Lena Ament and Ana Ivonne Vazquez-Armendariz, PhD / AG Herold. This image was acquired with a 25x water/1.0NA objective at a 2-photon excitation of 1045nm. Upon stitching, the final volume was deconvolved with the Huygens Essential software and rendered with Huygens SFP Renderer. Image acquired and post-processed by Dr. Ioannis Alexopoulos.
2nd Prize Winner
Image from Blake Hernandez
Maximum intensity projection of Huygens deconvolved Leica SP8 confocal image of pre-implantation mouse embryo showing actin (orange), microtubules (gray), and chromosomes (cyan).
3rd Prize Winner
Image from Maaike Lambers
Kinetochores and microtubules engage in various interactions during mitosis. When treated with a low drug concentration, their shapes resemble coral. This cell was imaged using expansion microscopy on a Zeiss LSM900 with AiryScan 2, and was then deconvolved using Huygens. Shown is a MIP rendering of the final data.
4th Prize Winner
Image from Rolando Berlinguer Palmini
Quote:"Technically challenging 2 colour STED large volume of a HeLa cell in anaphase stained for Tubulin (red), TOM20 (green - mitochondria) and DNA (DAPI – Blue – Confocal). One of the main problem with STED is bleaching and sometimes the fluorophores are damaged even at the first optical slice. The more dyes and optical channels, the more difficult to avoid bleaching. Here we managed to get 72(!) optical slices for a total Z depth of 12.09 um. We used the not-setting “Slowfade glass” mounting media to preserve the 3D shape. Within the SFP volume rendered image I noticed how beautiful the chromosome were rendered. They looked fluffy and ethereal still they contain the code of life. The mitochondria are scientifically and educationally very interesting because of the distribution around the nucleus during this high energy demanding phase. Tubulin is encasing the chromosomes."
5th Prize Winner
Image from Christian Jüngst
Superresolution STED image of mitochondrial cristae labelled with PKMO. Huygens was used for deconvolution of the image.
2021 Winners
- 1st Prize: Dr. Rolando Berlinguer Palmini (BioImaging Unit) and Dr. Christin Albus (Mitochondria Research Group), Newcastle University, UK
- 2nd Prize: Dr. Claudio Retamal, CEBICEM, Facultad de Medicina y Ciencia, Universidad San Sebastian, Santiago, Chile
- 3rd Prize: Dr. Grazvydas Lukinavicius, MPI for Biophysical Chemistry - Department of NanoBiophotonics, Max Planck Institute, Germany.
- 4th Prize: Dr, Alberto Moreno Cencerrado (Institute of Molecular Pathology) and Gabriele Bradamante (Gregor Mendel Institute)) and , Austria
- 5th Prize: Dr. Daniela Malide NHLBI Light microscopy core facility, NIH Bethesda, USA
1st Prize Winner
Image from Rolando Berlinguer Palmini and Christin Albus
"Christmas Lights & Christmas Tree" - Challenging 4 colour STED 3D stack combined with RNA FISH! Leica STED image was deconvolved and visualized with Huygens Professional! U2OS cells with mitochondrial outer membrane Tom20 (AF488 - White), ND1 mRNA FISH Quasar 570 ND1 NADH dehydrogenase subunit 1 (Green), ND2 mRNA FISH CalFluor 610 NADH dehydrogenase 2 (ND2) protein (Red), mitochondrial RNA-binding protein GRSF1 (RNA granule) - Abberior star red (Blue). Tom20 is MIP rendered (white) and other channels are surface rendered with Huygens.
2nd Prize Winner
Image from Claudio Retamal
HeLa cell treated with a PKA inhibitor, stained for EGFR (red) Transferrin (green) Rab11 (blue) and DAPI (light cyan). This image, acquired with a Leica SP8 CLSM, was deconvolved, chromatic aberration corrected and 3D surface rendered with the Huygens Software. Image published as the October issue cover of Traffic Journal.
3rd Prize Winner
Image from Grazvydas Lukinavicius
Large FOV of living U-2 OS cells stained with mitochondria (red-hot), tubulin (cyan) and actin (grey) probes. This confocal tile scan was acquired on the Abberior Facility Line, and was deconvolved and stitched using Huygens Essential.
4th Prize Winner
Image Gabriele Bradamante and Alberto Moreno Cencerrado
Virus-infected Arabidopsis flower bud - 3D MIP rendering. Violet: TuMV-6K2-Scarlet. Green: pUb::H2B-Clover. A set of eight images, each acquired from a different angle with a Zeiss Lightsheet Z.1 using a 10X water objective, were deconvolved, fused and visualized using Huygens Professional.
5th Prize Winner
Image from Daniela Malide
Mitochondria in COS7 cells stained for Tom20 were imaged as a tile-z-stack with a Leica SP8 STED 3X. The image was deconvolved, surface-rendered, and segmented in Huygens (numbers label individual objects in Huygens Object Analyzer).
2020 Winners
- 1st Prize: Dr. Juraj Kabat, Dr. Olena Kamenyeva, and Dr. Steven Brooks, NIAID/NIH, Bethesda, USA
- 2nd Prize: Dr. Barbora Kabatova, Dr. Juraj Kabat and Dr Bo Liang, NIAID/NIH, Bethesda, USA
- 3rd Prize: Dr. Rolando Berlinguer Palmini (BioImaging Unit) and Dr. Matthew Zorkau (Mitochondria Research Group), Newcastle University
- 4th Prize: Dr. Zhiye Lu, Dr. Daniela Malide, Dr. Xuefei Ma, NHLBI Light microscopy core facility, NIH Bethesda, USA
- 5th Prize: Dr. Olena Kamenyeva and Dr. Juraj Kabat, Dr. Simon Wabitsch and Dr. Tim Greten, NIAID/NIH Bethesda, USA
1st Prize Winner
Image from Juraj Kabat, Olena Kamenyeva and Steven Brooks
High quality and SFP rendered multiphoton image of Alpha Globin in human arteries. Fluorescent reporters: Red, collagen (SHG); Green, elastin; Blue, Alpha Globin. This 3D stack was acquired on a Leica SP8 DIVE using a 25x objective. Huygens Professional was used to align the data with the Object Stabilizer, and to deconvolve and 3D-visualize the image with the SFP Volume Renderer.
2nd Prize Winner
Image from Barbora Kabatova, Juraj Kabat and Bo Liang
Cell infected with human respiratory syncytial virus with Green Fluorescent Protein (RSV-GFP in green) within a culture of differentiated mucociliary Human airway epithelial cells. Cells were fixed and stained with DAPI to visualize nuclei (in blue), and antibodies against β-tublin for cilia (in red) and against the chemokine receptor CX3CR1 (in yellow). This 3D Leica SP8 confocal (40x) image was aligned using Huygens Object Stabilizer, crosstalk reduced using Huygens Crosstalk Corrector, deconvolved in Huygens Professional, and visualized with Huygens MIP Renderer.
3rd Prize Winner
Image from Rolando Berlinguer Palmini and Matthew Zorkau
This has proven to be a crucial image to show the submitochondrial location of newly synthesised proteins. The green rendered fluorescent signal represents newly synthesised mitochondrial protein and the red is an immunofluorescent antibody to a mitochondrial protein found in the inner boundary membrane of the mitochondrion (TIM23). This Huygens deconvolved image visualized with Huygens Surface Renderer shows a section of the human mitochondrial network taken at STED nanoscopy resolution using AF594 depleted with a 775nm STED laser and AF532 depleted with a 660nm STED laser.
4th Prize Winner
Image from Zhiye Lu, Daniela Malide and Xuefei Ma
3D maximum intensity projection of the nervous system of a iDISCO-cleared mouse embryo imaged on a Zeiss 880 confocal and stitched. The image was rendered using Huygens Maximum Intensity Projection (MIP) renderer with depth-coded coloring in Z.
5th Prize Winner
Movie from Olena Kamenyeva, Juraj Kabat, Simon Wabitsch and Tim Greten
CXCR6-GFP reporter cells (green) attack cancer (red) after arriving from blood vessels in mouse liver (blue and purple). Intravital microscopy with a Leica DIVE microscope was used to acquire and stitch 8 tile images (total tissue depth of 40 μm). Post-acquisition processing involved correction of artificial motion (transmitted heartbeat), image stabilization, and deconvolution using Huygens Professional software.
2019 Winners
- 1st Prize: Howard Vindin, PhD candidate, Weiss Lab, Charles Perkins Centre, The University of Sydney, NSW, Australia
- 2nd Prize: Dr. Marta Cortes Canteli, Miguel Servet Research Fellow, Centro Nacional de Investigaciones Cardiovasculares Carlos III, Spain.
- 3rd Prize: Mrs. Karin Panser, Pauli Group, Institute of Molecular Pathology, Austria.
- 4th Prize: Dr. Grazvydas Lukinavicius, MPI for Biophysical Chemistry - Department of NanoBiophotonics, Max Planck Institute, Germany.
- 5th Prize: Dr. Ioannis Alexopoulos (General Instrumentation), sample provided by Dr. Ivo Rieu & Prof. Dr. Jian Xu and prepared by Mieke Wolters (Molecular Plant Physiology), Faculty of Science, Radboud University, Netherlands.
1st Prize Winner
Image from Howard Vindin
This single channel 350GB image shows Erythrocytes that mark the developing vasculature in a mouse embryo (E14.5). The 8x11x2mm specimen was imaged on a multiphoton microscope excited at 790nm using a 25x 1.0NA Objective. Subsequently, the image was stitched, deconvolved with Huygens Professional using a measured PSF, and visualised with depth-coded colouring using the Huygens MIP renderer (version 19.10). Howard's instagram account (#artofmicroscopy) shows many great images and nearly all of them have been processed with the help of Huygens .
2nd Prize Winner
Image from Marta Cortes Canteli
This Huygens deconvolved image shows hypertrophic and reactive astrocytes (GFAP-green) present in the brain parenchyma of transgenic Alzheimer’s disease mice. The confocal z-stack was acquired according to Nyquist criteria using a HC PL APO 93X/1.30 GLYC motCORR objective of a Leica TCS SP8 Confocal-gSTED 3D System. The data was deconvolved with Huygens Professional. Finally, a 3D surface was obtained using the SFP Volume Renderer of Huygens Professional Software. Isosurface of the green channel was applied as indicated.
3rd Prize Winner
Image from Karin Panser
This Huygens deconvolved image shows an optical section through somites of a 2-day old zebrafish tail, stained for actin (phalloidin, shown in orange-gold) and nuclei (DAPI, shown in blue). The image was acquired on a Zeiss LSM700 confocal (40x, 1.3 NA) and deconvolved with Huygens Professional.
4th Prize Winner
Image from Grazvydas Lukinavicius
This Huygens deconvolved image shows a IsoSTED image of tubulin labelled with a small molecule probe, and imaged on an Abberior STED expert line microscope. Confocal and 3D STED images were deconvolved using Huygens software. Movie generated using Huygens MIP renderer.
5th Prize Winner
Image from Ioannis Alexopoulos
Multiview light sheet data (3 angles: -135deg, 45deg, 135 degrees) was fused and deconvolved with Huygens FUSER, and shows Arabidopsis thaliana mature anther with pollen grains, stained with Alexander's staining protocol. Multiview images were taken with an Olympus/PhaseView Alpha3 Light Sheet system. Image was visualized with the Huygens MIP Renderer using depth-code colouring.
2018 Winners
- 1st Prize: Dr. Outi Paloheimo. Tampere Imaging Facility, University of Tampere, Finland. Special thanks to the Heart Group, Faculty of Medicine and Health Technology, University of Tampere for providing the cells.
- 2nd Prize: Dr. Howard Vindin, Cell Biology Group, The Woolcock Institute of Medical Research, The University of Sydney, Australia. Special thanks also to Sydney Microscopy and Microanalysis, ACMM, University of Sydney.
- 3th Prize: Dr. Grazvydas Lukinavicius, Department of Nanobiophotonics, Max Planck Institute for Biophysical Chemistry, Germany.
1st Prize Winner
Image from Outi Paloheimo
This Huygens deconvolved confocal image shows Human induced pluripotent stem cell derived cardiomyocytes (heart cells) with filamentous actin in red, and nuclei in gray. The image was acquired with a Zeiss LSM780 microscope with a 63x/1.40 oil immersion objective, 561 nm and 405 nm laser lines. Scaling X, Y 0.047 µm, scaling Z 0.150 µm (z range 8.40 µm). Image size 192x192 µm (xy). Deconvolution was performed with Huygens Essential (18.04) using a theoretical PSF and the CMLE algorithm.
2nd Prize Winner
Movie submitted by Howard Vindin
Autofluorescence of thick elastic fibers (red) and SHG signal (collagen, green) in part of the Pulmonary pleurae from a human lung. The image was acquired on a Leica SP8 two photon microscope (63x 1.4NA), deconvolved with Huygens Professional and visualized using the Huygens SFP renderer. Stack dimensions are 84x84x18 μm.
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3rd Prize
Image from Grazvydas Lukinavicius
Huygens deconvolved image of fruit fly tissue stained with Tubulin probe (magenta) and tracheole (yellow). This high resolution and quality image was acquired using a STED 775 QUAD scanning microscope (Abberior Instruments GmbH).
2017 Winners
- 1st Prize: Dr. Romain Guiet, BioImaging & Optics Platform – EPFL, Lausanne, Switzerland
- 1st Prize: Dr. Dimitris Kapsokalyvas, Department of Molecular Cell Biology, Maastricht University,The Netherlands
- 3rd Prize: Dr. Tagide DeCarvalho, Department of Biological Sciencess, University of Maryland, Baltimore County, USA.
- 4th Prize: Dr. Gokhan Yilmaz, Department of Pharmacology, University of Oxford, UK.
- 5th Prize: Dr. Motosuke Tsutsumi, Nikon Imaging Center at Hokkaido University, Japan
1st Prize Winner
Image from Romain Guiet
Hela cell stained for DNA (Azure), F-Actin (Spring Green), Mitochondria (Amber) and Tubulin (Bright Pink). Confocal images were taken with a Zeiss LSM710 microscope and deconvolved with Huygens software.
1st Prize Winner
Image submitted by Dimitris Kapsokalyvas
SHG signal of the rat soleous muscle's myosin imaged with a Leica two-photon microscope (NA: 1, 20x). Stack has been deconvolved with Huygens using a measured PSF, and visualized with the Huygens SFP Renderer. High quality imaging together with Huygens allows you to see through the muscle's A bands from one side to the other. The stack dimensions is 105x105x87 μm.
3rd Prize
Image in the category "Tissue and Organisms", from Tagide DeCarvalho
This image of a cyanobacteria mat/biofilm, which is stained with acridine orange, shows much color that is mostly due to autofluorescence. This aesthetic image was acquired on a Leica confocal, and deconvolved and MIP rendered with Huygens. It could well have been a product of modern art.
4th Prize
Image submitted by Gokhan Yilmaz
This colorful picture is a high-resolution image of Niemann-Pick Disease Type C (NPC) cells taken with a Leica STED using 100% 775 STED depletion. It shows after deconvolution with Huygens much detail and striking weak filopodia formation in the NPC cells.
5th Prize
Movie submitted by Motosuke Tsutsumi
This movie was made with Huygens and shows fixed HeLa cells stained with Hoechst 33342 and alpha-tubulin. The 3D image was acquired with a Nikon A1 confocal (60x, NA 1.4) and deconvolved using Huygens Essential Deconvolution Express.
2016 Winners
- 1st Prize: Dr. Daniela Malide, Light Microscopy Core Facility of the NIH - National Heart, Blood and Lung Institute, Bethesda, USA.
- 1st Prize: Mrs. Outi Paloheimo from the Neuro Group BioMediTech, and Imaging Facility, University of Tampere, Finland.
- 3rd Prize: Dr. Priyam Banerjee, MD Anderson Cancer Center, Houston, Texas, USA.
- 4th Prize: Mrs. Julia Sauerwald, Group of Prof. Stefan Luschnig, Institute for Neurobiology, WWU Muenster, Germany.
- 5th Prize: Dr. Eva Wegel, JIC BioImaging, John Innes Centre, Norwich, United Kingdom.
1st Prize Winners
Image in the category "Cells", from Daniela Malide
COS-7 (fibroblast-like) cell line with mitochondria in green/white and cytoskeletal protein tubulin in red/magenta. Comparing the diffraction limited confocal image (green/red) with the super-resolution STED (Stimulated Emission Depletion) microscopy image (white/magenta). STED reveals thin tubulin strands (magenta) and details of the TOM-20 stained outer mitochondria membrane (white). Images were taken with a Leica SP8 STED 3X microscope and deconvolved with Huygens software.
Image in the category "Tissue and Organisms", from Outi Paloheimo
The image represents a portion of the wing (showing arrangement of scales) of Pieris brassicae (cabbage butterfly). A Zeiss LSM 780 confocal microscope (25x/0.8 objective) with excitation lasers 488 nm, 535 nm, 633 nm was used to image the autofluorescence. The image was deconvolved using Huygens Essential (CMLE and theoretical PSF).
3rd Prize
Image submitted by Priyam Banerjee
Human lung adenocarcinoma tissue with the extracellular matrix protein Collagen I immunostained in red (Alexa Fluor 568), collagen modifying enzyme Lysine Hydroxylase II (LH2) immunostained in green (Alexa Fluor 488). Nuclei were counterstained in blue (DAPI). Image was acquired with a Nikon A1+ confocal using Plan Apo 10X 0.45 NA objective. The image was deconvolved and SFP rendered with Huygens Professional version 16.10
4th Prize
Image submitted by Julia Sauerwald
The image shows a Drosophila thorax captured with a Zeiss 880 confocal microscope and deconvolved using Huygens Essential. Respiratory tracheal branches are labeled in various colors using stochastic expression of spaghetti monster GFP with different epitope tags.
5th Prize
Image submitted by Eva Wegel
The image is a maximum intensity projection (MIP) of a z-stack through a Drosophila macrophage imaged on a Leica TCS SP8X scanning confocal microscope. Objective NA 1.4. Pinhole size 405nm 0.17 AU, 488nm 0.15 AU, 568nm 0.15 AU for obtaining the best possible resolution.
Nuclei are DAPI stained (cyan), alpha-tubulin was detected with a primary mouse DM1A antibody and a secondary anti-mouse antibody coupled to Alexa Fluor 488 (magenta), actin was labelled with phalloidin coupled to Alexa Fluor 568 (green). Deconvolution was done with CMLE using Huygens Essential default settings.
2015 Winners
- 1st Prize: Dr. Pawel Pasierbek, BioOptics Facility of the IMP-IMBA-GMI, Vienna, Austria
- 2nd Prize: Dr. Matyas Molnar, BioVis Facility, Uppsala University, Sweden
- 3rd Prize: Dr. Helfrid Hochegger, Genome and Stability Centre, University of Sussex, UK
- 4th Prize: Dr. Arndt Meyer, Animal Navigation Group, University of Oldenburg, Germany
- 5th Prize: Dr. Jorge Bernardino de la Serna, Science and Technology Facilities, Rutherford Appleton Laboratory, UK
- 6th Prize: Dr. Jing Yan, Department of Molecular Biology, Princeton University, USA
1st Prize
Image from Pawel Pasierbek, BioOptics (IMP, IMBA, GMI), Vienna, Austria.
Download the full size image here
Spinning disk confocal image of tissue culture neiurons deconvolved with Huygens professional.
2nd Prize
Image from Matyas Molnar from the BioVis imaging facility, Uppsala University, Sweden.
Download the full size image here
''Ant head autofluorescence captured with a Zeiss 710 confocal microscope using 488nm laser excitation and detection of two channes (blue and green). The acquired 3D dataset was deconvolved and maximum intensity projection image was rendered with Huygens. }
3rd Prize
Image submitted by Helfrid Hochegger, Genome and Stability Centre, Sussex Universty, UK.
Download the full size image here
The image shows glioma stem cells grown on matrigel and stained by IF
with tubulin (green, actin (red), centromeres/CREST (white) and DAPI (blue). The image was taken on an Olympus IX73 using a 40x 0.9NA. }
4th Prize
Image submitted by Arndt Meyer, Animal Navigation Group, University of Oldenburg, Germany.
Download the full size image here
Calbindin immunoreactivity in the ganglion cell layer of a mouse retina. The image was taken close to the center of the retina, where the ganglion cell axons gather in thick bundles and then leave the eye as the optic nerve. This confocal stack was recorded on a Leica SP8 microscope, deconvolved using Huygens Essential, and finally color-coded for depth.
5th Prize
Image submitted by Jorge Bernardino Rutherford Appleton Laboratory, UK.
Download the full size image here
Image of a T lymphocyte crawling taken with a Leica SP8 g-STED.
The image is deconvolved with Huygens and the final visual effect was obtained using the Huygens surface rendering tool.
Blue shows labelled plasma membrane with a specific lipophilic dye, red represents the actin filaments, and yellow internal cytosolic vesicles.
6th Prize
Image submitted by Jing Yan, Princeton University, USA.
Download the full size image here
Image shows a growing community of bacteria Vibrio cholerae, the pathogen for cholerae. Bacteria adopt a social life form known as biofilm, where they stay together and secrete chemicals to build a "home" for survival. This Nikon spinning disc confocal image was deconvolved with a theoretical PSF in Huygens and finally color coded for depth.
2014 Winners
1st Prize
Image from Imre Gaspar of the EMBL Heidelberg using the Leica SP8 and Huygens Remote Manager/Core at the Advanced Light Microscopy Facility, Germany.
The image represents a Z-stack of 116 sections showing a series of developing Drosophila oocytes with actin in yellow (Phalloidin) and the nuclear envelope of the nurse cells in green (GFP-Tm1).
2nd Prize
Seema S. Lakdawala and Juraj Kabat of the National Institute of Allergy and Infectious Disease (NIAID), NIH, Bethesda, USA: This Leica SP5 confocal image was deconvolved with Huygens.
The image visualizes a MDCK cell that was infected with influenza A H1N1 virus and stained with fluorescent probes targeting 4 distinct influenza viral RNA segments, PB2 (red), PB1 (green), PA (orange), and NP (yellow). The nucleus is labeled in blue based on DAPI staining.
3rd Prize
Leica SP8 confocal image from Yury Belyaev of the ALMF-EMBL Heidelberg (Germany). The image was found and selected using Huygens Titan, and deconvolved and visualized with Huygens Remote Manager and Core.
The image was acquired with a Leica SP8 confocal with a water objective (NA 1.1) and represents a fish eye with membrane in green and nuclei in red.
2013 Winners
1st Prize
Image from Karin Panser from the laboratory of Dr. Andrew Straw, Institute of Molecular Pathology (I.M.P.), Vienna, Austria.
The image represents fruit fly (Drosophila melanogaster) ommatidia, which are arranged in an extremely regular array in the compound eye. Nuclei are shown in blue (DAPI), cadherin in red, and chaoptin in the photoreceptors in green. This Zeiss LSM780 confocal (NA 1.3, 40x) image was deconvolved with Huygens Professional.
2nd Prize
Dr. Ulrike Engel, Nikon Imaging Center, BioQuant Institute, Heidelberg, Germany
Huygens deconvolved and MIP rendered confocal image (Nikon; NA 0.45) of a tadpole intestine with nuclei in orange and muscle actin in cyan. The direction of the gut looping can be used as a readout for proper asymmetric organ development. Looping in the other direction is a sign of perturbed Nodal/Notch signaling.
3rd Prize
Matthew Mitschelen from the Reynolds Oklahoma Center on Aging, University of Oklahoma Health Sciences Center, USA
Huygens deconvolved and MIP rendered epifluorescence Z stack of part of a mouse brain. The image shows aquaporin 4 (red) as individual astrocytic end-feet along a blood vessel. Thanks to deconvolution, GFAP (green) can be colocalized with AQ4 in small areas, but the end-feet and arms of astrocytes can be identified as distinguishable structures in terms of protein expression.