Automated Organization ProfileMax Perutz Labs
Max Perutz Labs
Current S-Index
Sum of Dataset Indices for all datasets
Average Dataset Index per Dataset
Average Dataset Index per dataset
Total Datasets
Total datasets in this organization
Average FAIR Score
Average FAIR Score per dataset
Total Citations
Total citations to the organization's datasets
Total Mentions
Total mentions of the organization's datasets
S-Index Interpretation
The S-Index (Sharing Index) is a comprehensive metric that represents the cumulative impact of all your datasets. It is calculated as the sum of Dataset Index scores across all your claimed datasets.
What it means:
- A higher S-index indicates greater overall impact of your datasets relative to typical datasets in their fields of research
- The S-Index grows as you add more datasets or as existing datasets gain more citations and mentions
- It provides a single number to track your research data impact over time
Current S-Index: 18.8 (sum of 15 datasets Dataset Index scores)
More information here.
S-Index Over Time
Cumulative Citations Over Time
Cumulative Mentions Over Time
Datasets
These datasets are the averaged reconstructions of cytokinesis in six steps that were produced by applying Zach Marin's 'Cytokinesis Pseudotime Analysis' package (https://github.com/zacsimile/cytokinesis-pseudotime-analysis) on a collection of 1930 fluorescence spinning disk confocal images. The data are fluorescence images of expanded NRK49F cells, undergoing cytokinesis. The images were acquired as z-stacks with 1 µm spacing and a X/Y-pixel size of 90 nm on a spinning disk confocal microscope.Applying an averaged expansion factor of 4.444, this results in an effective X/Y pixel size of 20.25 nm and 225 nm in Z-direction. These properties can be adjusted for the correct representation of the averaged reconstructions when opening the files in FIJI/ImageJ.The files are composed of 6 time points, representing 6 differet stages of cytokinesis (RC, CS, RS, SM, BA, A).The files are referenced as Supplementary Files 1-4 in the associated preprint. The table below summarizes the file details.z-stack is a volumetric averagemean-proj is a 2D mean projected averageradial-proj is the axio-radial distribution along the main axis of the cytokinetic bridgeFileFile nameDescriptionSupplementary File 1pseudotime_images_z-stack_reduced_MTs_sen_DAI_Cek_MK1_Ra1_PR1_CiK_ann_myA_myB_acn_Se7_Se1_Se9_BO4_Tsm_ALm_IS1_CHB_16bit.tif5D file including all targets that were analyzed and averaged in this study in the 6 cytokinetic stages (order: RC, CS, RS, SM, BA, A)Supplementary File 2pseudotime_images_mean-proj_MTs_sen_DAI_Cek_MK1_Ra1_PR1_CiK_ann_myA_myB_acn_Se7_Se1_Se9_BO4_Tsm_ALm_IS1_CHB_16bit.tif4D file, mean projections of all targets that were analyzed and averaged in this study in the 6 cytokinetic stages (order: RC, CS, RS, SM, BA, A)Supplementary File 3pseudotime_images_radial-proj_MTs_sen_DAI_Cek_MK1_Ra1_PR1_CiK_ann_myA_myB_acn_Se7_Se1_Se9_BO4_Tsm_ALm_IS1_CHB_16bit.tif4D file, axio-radial projections of all targets that were analyzed and averaged in this study in the 6 cytokinetic stages (order: RC, CS, RS, SM, BA, A)Supplementary File 4pseudotime_images_mean-proj_MTs_sen_DAI_IS1_CHB_16bit.tif4D file, mean projections of the sub-stages of ESCRT-III cone assembly (order: RC, CS, RS, SM0, SM1, SM2, SM3, BA0, BA1, BA2, BA3, BA4, A)The order of the channels in Suppl. Files 1-3 is as followsMTs tubulinsen Septin2-GFPDAI DAPICek CellMask orangeMK1 MKLP1Ra1 MgcRacGAP1PR1 PRC1CiK Citron Kinaseann AnillinmyA Myosin IIAmyB Myosin IIBacn actinSe7 Septin7 Se1 Septin11Se9 Septin9BO4 BORG4Tsm Tsg101ALm ALIXIS1 IST1CHB CHMP4B
Authors
- Hümpfer, Nadja ;
- Marin, Zach ;
- Bruckmann, Kjell ;
- Ries, Jonas ;
- Ewers, Helge
These datasets are the averaged reconstructions of cytokinesis in six steps that were produced by applying Zach Marin's 'Cytokinesis Pseudotime Analysis' package (https://github.com/zacsimile/cytokinesis-pseudotime-analysis) on a collection of 1930 fluorescence spinning disk confocal images. The data are fluorescence images of expanded NRK49F cells, undergoing cytokinesis. The images were acquired as z-stacks with 1 µm spacing and a X/Y-pixel size of 90 nm on a spinning disk confocal microscope.Applying an averaged expansion factor of 4.444, this results in an effective X/Y pixel size of 20.25 nm and 225 nm in Z-direction. These properties can be adjusted for the correct representation of the averaged reconstructions when opening the files in FIJI/ImageJ.The files are composed of 6 time points, representing 6 differet stages of cytokinesis (RC, CS, RS, SM, BA, A).The files are referenced as Supplementary Files 1-4 in the associated preprint. The table below summarizes the file details.z-stack is a volumetric averagemean-proj is a 2D mean projected averageradial-proj is the axio-radial distribution along the main axis of the cytokinetic bridgeFileFile nameDescriptionSupplementary File 1pseudotime_images_z-stack_reduced_MTs_sen_DAI_Cek_MK1_Ra1_PR1_CiK_ann_myA_myB_acn_Se7_Se1_Se9_BO4_Tsm_ALm_IS1_CHB_16bit.tif5D file including all targets that were analyzed and averaged in this study in the 6 cytokinetic stages (order: RC, CS, RS, SM, BA, A)Supplementary File 2pseudotime_images_mean-proj_MTs_sen_DAI_Cek_MK1_Ra1_PR1_CiK_ann_myA_myB_acn_Se7_Se1_Se9_BO4_Tsm_ALm_IS1_CHB_16bit.tif4D file, mean projections of all targets that were analyzed and averaged in this study in the 6 cytokinetic stages (order: RC, CS, RS, SM, BA, A)Supplementary File 3pseudotime_images_radial-proj_MTs_sen_DAI_Cek_MK1_Ra1_PR1_CiK_ann_myA_myB_acn_Se7_Se1_Se9_BO4_Tsm_ALm_IS1_CHB_16bit.tif4D file, axio-radial projections of all targets that were analyzed and averaged in this study in the 6 cytokinetic stages (order: RC, CS, RS, SM, BA, A)Supplementary File 4pseudotime_images_mean-proj_MTs_sen_DAI_IS1_CHB_16bit.tif4D file, mean projections of the sub-stages of ESCRT-III cone assembly (order: RC, CS, RS, SM0, SM1, SM2, SM3, BA0, BA1, BA2, BA3, BA4, A)The order of the channels in Suppl. Files 1-3 is as followsMTs tubulinsen Septin2-GFPDAI DAPICek CellMask orangeMK1 MKLP1Ra1 MgcRacGAP1PR1 PRC1CiK Citron Kinaseann AnillinmyA Myosin IIAmyB Myosin IIBacn actinSe7 Septin7 Se1 Septin11Se9 Septin9BO4 BORG4Tsm Tsg101ALm ALIXIS1 IST1CHB CHMP4B
Authors
- Hümpfer, Nadja ;
- Marin, Zach ;
- Bruckmann, Kjell ;
- Ries, Jonas ;
- Ewers, Helge
This archive contains raw Single Particle Tracking (SPT) data as exported from MINFLUX-iMSCPECTOR (commercial version - 16.3.15645-m2205) in the .npy file-format as well as SPT image stacks taken on a custom TIRF Microscope with custom control software. Information on the experimental conditions and sample generation are found within the related preprint The MINFLUX sequence files used to control the device are located in the related GitHub repository.Related preprint.Related GitHub repository.(Working title: "Parameter Optimization for MINFLUX Microscopy enabled Single Particle Tracking.")
Authors
- Vogler, Bela Tristan Leander ;
- De Angelis, Giovanni ;
- Zhao, Ziliang ;
- Eggeling, Christian ;
- Reina, Francesco
This archive contains raw Single Particle Tracking (SPT) data as exported from MINFLUX-iMSCPECTOR (commercial version - 16.3.15645-m2205) in the .npy file-format as well as SPT image stacks taken on a custom TIRF Microscope with custom control software. Information on the experimental conditions and sample generation are found within the related preprint The MINFLUX sequence files used to control the device are located in the related GitHub repository.Related preprint.Related GitHub repository.(Working title: "Parameter Optimization for MINFLUX Microscopy enabled Single Particle Tracking.")
Authors
- Vogler, Bela Tristan Leander ;
- De Angelis, Giovanni ;
- Zhao, Ziliang ;
- Eggeling, Christian ;
- Reina, Francesco
This file contains the source data used in Henggeler et al., organized by figure and figure panel for clarity.
Authors
- Matos, Joao ;
- Henggeler, Adrian
This file contains the source data used in Henggeler et al., organized by figure and figure panel for clarity.
Authors
- Matos, Joao ;
- Henggeler, Adrian
These datasets represent raw data for the preparation of Figures in:Ferraioli S, Sarigol F, Prakash C, Filipczak D, Foisner R, Naetar N. (2024) LAP2alpha facilitates myogenic gene expression by preventing nucleoplasmic lamin A/C from spreading to active chromatin regions. Nucleic Acids Res.2024 Sep 4:gkae752. doi: 10.1093/nar/gkae752.
Authors
- Sarigol, Fatih ;
- Foisner, Roland ;
- Naetar, Nana
These datasets represent raw data for the preparation of Figures in:Ferraioli S, Sarigol F, Prakash C, Filipczak D, Foisner R, Naetar N. (2024) LAP2alpha facilitates myogenic gene expression by preventing nucleoplasmic lamin A/C from spreading to active chromatin regions. Nucleic Acids Res.2024 Sep 4:gkae752. doi: 10.1093/nar/gkae752.
Authors
- Sarigol, Fatih ;
- Foisner, Roland ;
- Naetar, Nana
Mitochondria are fundamental for life and require balanced ion exchange to maintain proper functioning. The mitochondrial cation exchanger LETM1 sparks interest because of its pathophysiological role in seizures in the Wolf Hirschhorn Syndrome (WHS). Despite observation of sleep disorganization in epileptic WHS patients, and growing studies linking mitochondria and epilepsy to circadian rhythms, LETM1 has not been studied from the chronobiological perspective. Here we established a viable letm1 knock-out, using the diurnal vertebrate Danio rerio to study the metabolic and chronobiological consequences of letm1 deficiency. We report diurnal rhythms of Letm1 protein levels in wild-type fish. We show that mitochondrial nucleotide metabolism is deregulated in letm1-/- mutant fish, the rate limiting enzyme of NAD+ production is up-regulated, while NAD+ and NADH pools are reduced. These changes were associated with increased expression amplitude of circadian core clock genes in letm1-/- compared to wild-type under light/dark conditions, suggesting decreased NAD(H) levels as a possible mechanism for circadian system perturbation in Letm1 deficiency. Replenishing NAD pool may ameliorate WHS-associated sleep and neurological disorders.
Authors
- Dao, Pauline ;
- Tessmar-Raible, Kristin ;
- Nowikovsky, Karin
Many species synchronize their physiology and behavior to specific hours. It is commonly assumed that sunlight acts as the main entrainment signal for ~24h clocks. However, the moon provides similarly regular time information. Consistently, a growing number of studies have reported correlations between diel behavior and lunidian cycles. Yet, mechanistic insight into the possible influences of the moon on ~24hr timers remains scarce. We have explored the marine bristleworm Platynereis dumerilii to investigate the role of moonlight in the timing of daily behavior. We uncover that moonlight, besides its role in monthly timing, also schedules the exact hour of nocturnal swarming onset to the nights’ darkest times. Our work reveals that extended moonlight impacts on a plastic clock that exhibits <24h (moonlit) or >24h (no moon) periodicity. Abundance, light sensitivity, and genetic requirement indicate that the Platynereis light receptor molecule r-Opsin1 serves as a receptor that senses moonrise, whereas the cryptochrome protein L-Cry is required to discriminate the proper valence of nocturnal light as either moon- or sunlight. Comparative experiments in Drosophila suggest that cryptochrome’s principal requirement for light valence interpretation is conserved. Its exact biochemical properties differ, however, between species with dissimilar timing ecology. Our work advances the molecular understanding of lunar impact on fundamental rhythmic processes, including those of marine mass spawners endangered by anthropogenic change.
Authors
- Zurl, Martin ;
- Poehn, Birgit ;
- Krishnan, Shruthi ;
- Rokvic, Dunja ;
- Veedin Rajan, Vinoth Babu ;
- Schlichting, Matthias ;
- Orel, Lukas ;
- Coric, Aida ;
- Lucas, Robert ;
- Wolf, Eva ;
- Helfrich-Förster, Charlotte ;
- Raible, Florian ;
- Tessmar-Raible, Kristin