| Literature DB >> 27864765 |
Jos R Wendrich1, Sjef Boeren1, Barbara K Möller1,2, Dolf Weijers3, Bert De Rybel1,4,5.
Abstract
Individual proteins often function as part of a protein complex. The identification of interacting proteins is therefore vital to understand the biological role and function of the studied protein. Here we describe a method for the in vivo identification of nuclear, cytoplasmic, and membrane-associated protein complexes from plant tissues using a strategy of immunoprecipitation followed by tandem mass spectrometry. By performing quantitative mass spectrometry measurements on biological triplicates, relative abundance of proteins in GFP-tagged complexes compared to background controls can be statistically evaluated to identify high-confidence interactors. We detail the entire workflow of this approach.Keywords: Arabidopsis; GFP; Immunoprecipitation; Protein complex identification; Protein–protein interaction; Tandem mass spectrometry
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Year: 2017 PMID: 27864765 DOI: 10.1007/978-1-4939-6469-7_14
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745