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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...

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Autores principales: de Graaf, Sebastiaan C., Klykov, Oleg, van den Toorn, Henk, Scheltema, Richard A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2018
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.
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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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