| Literature DB >> 30520642 |
Andrew Keller1, Juan D Chavez1, Jimmy K Eng1, Zorian Thornton1, James E Bruce1.
Abstract
In cells, intra- and intermolecular interactions of proteins confer function, and the dynamic modulation of this interactome is critical to meet the changing needs required to support life. Cross-linking and mass spectrometry (XL-MS) enable the detection of both intra- and intermolecular protein interactions in organelles, cells, tissues, and organs. Quantitative XL-MS enables the detection of interactome changes in cells due to environmental, phenotypic, pharmacological, or genetic perturbations. We have developed new informatics capabilities, the first to enable 3D visualization of multiple quantitative interactome data sets, acquired over time or with varied perturbation levels, to reveal relevant dynamic interactome changes. These new tools are integrated within release 3.0 of our online cross-linked peptide database and analysis tool suite XLinkDB. With the recent rapid expansion in XL-MS for protein structural studies and the extension to quantitative XL-MS measurements, 3D interactome visualization tools are of critical need.Entities:
Keywords: cross-link database; cross-linking; dynamic interactome; heatmap; interaction surfaces; interactome movies; mass spectrometry; protein complexes; protein interaction networks; quantitative proteomics
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Year: 2018 PMID: 30520642 PMCID: PMC6519740 DOI: 10.1021/acs.jproteome.8b00703
Source DB: PubMed Journal: J Proteome Res ISSN: 1535-3893 Impact factor: 4.466