| Literature DB >> 32345597 |
Katrina Meyer1, Matthias Selbach2.
Abstract
Protein-protein interactions are often mediated by short linear motifs (SLiMs) that are located in intrinsically disordered regions (IDRs) of proteins. Interactions mediated by SLiMs are notoriously difficult to study, and many functionally relevant interactions likely remain to be uncovered. Recently, pull-downs with synthetic peptides in combination with quantitative mass spectrometry emerged as a powerful screening approach to study protein-protein interactions mediated by SLiMs. Specifically, arrays of synthetic peptides immobilized on cellulose membranes provide a scalable means to identify the interaction partners of many peptides in parallel. In this minireview we briefly highlight the relevance of SLiMs for protein-protein interactions, outline existing screening technologies, discuss unique advantages of peptide-based interaction screens and provide practical suggestions for setting up such peptide-based screens.Entities:
Keywords: Peptide array; affinity proteomics; high throughput screening; intrinsically disordered regions; mass spectrometry; peptide interactions; peptides; post-translational modifications; protein-protein interactions; short linear motifs
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Year: 2020 PMID: 32345597 PMCID: PMC7338088 DOI: 10.1074/mcp.R120.002034
Source DB: PubMed Journal: Mol Cell Proteomics ISSN: 1535-9476 Impact factor: 5.911