4.7 Article

Cross-ID: Analysis and Visualization of Complex XL-MS-Driven Protein Interaction Networks

Journal

JOURNAL OF PROTEOME RESEARCH
Volume 18, Issue 2, Pages 642-651

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jproteome.8b00725

Keywords

cross-linking mass spectrometry; XL-MS; complex protein mixtures; proteome-wide cross-linking; XlinkX; protein-protein interactions; DisVis; XL-TMT

Funding

  1. large-scale proteomics facility Proteins@Work embedded in The Netherlands Proteomics Centre [184.032.201]
  2. Netherlands Organization for Scientific Research (NWO)
  3. European Union Horizon 2020 program FET-OPEN project MSmed [686547]
  4. European Union Horizon 2020 program INFRAIA project Epic-XS [823839]

Ask authors/readers for more resources

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.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available