| Literature DB >> 33859439 |
Andrea Fossati1,2,3,4, Chen Li5,6, Federico Uliana1, Fabian Wendt7, Fabian Frommelt1, Peter Sykacek8, Moritz Heusel1,9, Mahmoud Hallal10, Isabell Bludau1,11, Tümay Capraz12, Peng Xue1,13, Jiangning Song14, Bernd Wollscheid7,15, Anthony W Purcell14, Matthias Gstaiger16, Ruedi Aebersold17,18.
Abstract
Despite the availability of methods for analyzing protein complexes, systematic analysis of complexes under multiple conditions remains challenging. Approaches based on biochemical fractionation of intact, native complexes and correlation of protein profiles have shown promise. However, most approaches for interpreting cofractionation datasets to yield complex composition and rearrangements between samples depend considerably on protein-protein interaction inference. We introduce PCprophet, a toolkit built on size exclusion chromatography-sequential window acquisition of all theoretical mass spectrometry (SEC-SWATH-MS) data to predict protein complexes and characterize their changes across experimental conditions. We demonstrate improved performance of PCprophet over state-of-the-art approaches and introduce a Bayesian approach to analyze altered protein-protein interactions across conditions. We provide both command-line and graphical interfaces to support the application of PCprophet to any cofractionation MS dataset, independent of separation or quantitative liquid chromatography-MS workflow, for the detection and quantitative tracking of protein complexes and their physiological dynamics.Entities:
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Year: 2021 PMID: 33859439 DOI: 10.1038/s41592-021-01107-5
Source DB: PubMed Journal: Nat Methods ISSN: 1548-7091 Impact factor: 28.547