Unknown

Dataset Information

0

CLMSVault: A Software Suite for Protein Cross-Linking Mass-Spectrometry Data Analysis and Visualization.


ABSTRACT: Protein cross-linking mass spectrometry (CL-MS) enables the sensitive detection of protein interactions and the inference of protein complex topology. The detection of chemical cross-links between protein residues can identify intra- and interprotein contact sites or provide physical constraints for molecular modeling of protein structure. Recent innovations in cross-linker design, sample preparation, mass spectrometry, and software tools have significantly improved CL-MS approaches. Although a number of algorithms now exist for the identification of cross-linked peptides from mass spectral data, a dearth of user-friendly analysis tools represent a practical bottleneck to the broad adoption of the approach. To facilitate the analysis of CL-MS data, we developed CLMSVault, a software suite designed to leverage existing CL-MS algorithms and provide intuitive and flexible tools for cross-platform data interpretation. CLMSVault stores and combines complementary information obtained from different cross-linkers and search algorithms. CLMSVault provides filtering, comparison, and visualization tools to support CL-MS analyses and includes a workflow for label-free quantification of cross-linked peptides. An embedded 3D viewer enables the visualization of quantitative data and the mapping of cross-linked sites onto PDB structural models. We demonstrate the application of CLMSVault for the analysis of a noncovalent Cdc34-ubiquitin protein complex cross-linked under different conditions. CLMSVault is open-source software (available at https://gitlab.com/courcelm/clmsvault.git ), and a live demo is available at http://democlmsvault.tyerslab.com/ .

SUBMITTER: Courcelles M 

PROVIDER: S-EPMC5994346 | biostudies-literature | 2017 Jul

REPOSITORIES: biostudies-literature

altmetric image

Publications

CLMSVault: A Software Suite for Protein Cross-Linking Mass-Spectrometry Data Analysis and Visualization.

Courcelles Mathieu M   Coulombe-Huntington Jasmin J   Cossette Émilie É   Gingras Anne-Claude AC   Thibault Pierre P   Tyers Mike M  

Journal of proteome research 20170605 7


Protein cross-linking mass spectrometry (CL-MS) enables the sensitive detection of protein interactions and the inference of protein complex topology. The detection of chemical cross-links between protein residues can identify intra- and interprotein contact sites or provide physical constraints for molecular modeling of protein structure. Recent innovations in cross-linker design, sample preparation, mass spectrometry, and software tools have significantly improved CL-MS approaches. Although a  ...[more]

Similar Datasets

| S-EPMC4977572 | biostudies-literature
| S-EPMC3859183 | biostudies-other
| S-EPMC3940544 | biostudies-literature
| S-EPMC6107636 | biostudies-literature
| S-EPMC4927332 | biostudies-literature
| S-EPMC6442367 | biostudies-literature
| S-EPMC6736138 | biostudies-literature
| S-SCDT-EMBOJ-2020-106174 | biostudies-other
| S-EPMC7883291 | biostudies-literature
| S-EPMC4359615 | biostudies-literature