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Cross-ID: Analysis and Visualization of Complex XL–MS-Driven Protein Interaction Networks
[Image: see text] Protein interactions enable much more complex behavior than the sum of the individual protein parts would suggest and represents a level of biological complexity requiring full understanding when unravelling cellular processes. Cross-linking mass spectrometry has emerged as an attr...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6407916/ https://www.ncbi.nlm.nih.gov/pubmed/30575379 http://dx.doi.org/10.1021/acs.jproteome.8b00725 |
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author | de Graaf, Sebastiaan C. Klykov, Oleg van den Toorn, Henk Scheltema, Richard A. |
author_facet | de Graaf, Sebastiaan C. Klykov, Oleg van den Toorn, Henk Scheltema, Richard A. |
author_sort | de Graaf, Sebastiaan C. |
collection | PubMed |
description | [Image: see text] Protein interactions enable much more complex behavior than the sum of the individual protein parts would suggest and represents a level of biological complexity requiring full understanding when unravelling cellular processes. Cross-linking mass spectrometry has emerged as an attractive approach to study these interactions, and recent advances in mass spectrometry and data analysis software have enabled the identification of thousands of cross-links from a single experiment. The resulting data complexity is, however, difficult to understand and requires interactive software tools. Even though solutions are available, these represent an agglomerate of possibilities, and each features its own input format, often forcing manual conversion. Here we present Cross-ID, a visualization platform that links directly into the output of XlinkX for Proteome Discoverer but also plays well with other platforms by supporting a user-controllable text-file importer. The platform includes features like grouping, spectral viewer, gene ontology (GO) enrichment, post-translational modification (PTM) visualization, domains and secondary structure mapping, data set comparison, previsualization overlap check, and more. Validation of detected cross-links is available for proteins and complexes with known structure or for protein complexes through the DisVis online platform (http://milou.science.uu.nl/cgi/services/DISVIS/disvis/). Graphs are exportable in PDF format, and data sets can be exported in tab-separated text files for evaluation through other software. |
format | Online Article Text |
id | pubmed-6407916 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-64079162019-03-11 Cross-ID: Analysis and Visualization of Complex XL–MS-Driven Protein Interaction Networks de Graaf, Sebastiaan C. Klykov, Oleg van den Toorn, Henk Scheltema, Richard A. J Proteome Res [Image: see text] Protein interactions enable much more complex behavior than the sum of the individual protein parts would suggest and represents a level of biological complexity requiring full understanding when unravelling cellular processes. Cross-linking mass spectrometry has emerged as an attractive approach to study these interactions, and recent advances in mass spectrometry and data analysis software have enabled the identification of thousands of cross-links from a single experiment. The resulting data complexity is, however, difficult to understand and requires interactive software tools. Even though solutions are available, these represent an agglomerate of possibilities, and each features its own input format, often forcing manual conversion. Here we present Cross-ID, a visualization platform that links directly into the output of XlinkX for Proteome Discoverer but also plays well with other platforms by supporting a user-controllable text-file importer. The platform includes features like grouping, spectral viewer, gene ontology (GO) enrichment, post-translational modification (PTM) visualization, domains and secondary structure mapping, data set comparison, previsualization overlap check, and more. Validation of detected cross-links is available for proteins and complexes with known structure or for protein complexes through the DisVis online platform (http://milou.science.uu.nl/cgi/services/DISVIS/disvis/). Graphs are exportable in PDF format, and data sets can be exported in tab-separated text files for evaluation through other software. American Chemical Society 2018-12-21 2019-02-01 /pmc/articles/PMC6407916/ /pubmed/30575379 http://dx.doi.org/10.1021/acs.jproteome.8b00725 Text en Copyright © 2018 American Chemical Society This is an open access article published under a Creative Commons Non-Commercial No Derivative Works (CC-BY-NC-ND) Attribution License (http://pubs.acs.org/page/policy/authorchoice_ccbyncnd_termsofuse.html) , which permits copying and redistribution of the article, and creation of adaptations, all for non-commercial purposes. |
spellingShingle | de Graaf, Sebastiaan C. Klykov, Oleg van den Toorn, Henk Scheltema, Richard A. Cross-ID: Analysis and Visualization of Complex XL–MS-Driven Protein Interaction Networks |
title | Cross-ID: Analysis
and Visualization of Complex XL–MS-Driven
Protein Interaction Networks |
title_full | Cross-ID: Analysis
and Visualization of Complex XL–MS-Driven
Protein Interaction Networks |
title_fullStr | Cross-ID: Analysis
and Visualization of Complex XL–MS-Driven
Protein Interaction Networks |
title_full_unstemmed | Cross-ID: Analysis
and Visualization of Complex XL–MS-Driven
Protein Interaction Networks |
title_short | Cross-ID: Analysis
and Visualization of Complex XL–MS-Driven
Protein Interaction Networks |
title_sort | cross-id: analysis
and visualization of complex xl–ms-driven
protein interaction networks |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6407916/ https://www.ncbi.nlm.nih.gov/pubmed/30575379 http://dx.doi.org/10.1021/acs.jproteome.8b00725 |
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