| Literature DB >> 32046850 |
Ashish Srivastava1, Mithu Baidya1, Hemlata Dwivedi-Agnihotri1, Arun K Shukla2.
Abstract
β-arrestins (βarrs) are multifunctional proteins that interact with activated and phosphorylated G protein-coupled receptors (GPCRs) to regulate their signaling and trafficking. Understanding the intricate details of GPCR-βarr interaction continues to be a key research area in the field of GPCR biology. Bimane fluorescence spectroscopy has been one of the key approaches among a broad range of methods employed to study GPCR-βarr interaction using purified and reconstituted system. Here, we present a step-by-step protocol for labeling βarrs with monobromobimane (mBBr) in a site-directed fashion for measuring their interaction with GPCRs and the resulting conformational changes. This simple protocol can be directly applied to other protein-protein interaction modules as well for measuring interactions and conformational changes in reconstituted systems in vitro.Entities:
Keywords: Biased agonism; Bimane; Drug discovery; Fluorescence spectroscopy; GPCRs; Protein–protein interaction; β-Arrestins
Mesh:
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Year: 2019 PMID: 32046850 PMCID: PMC7217711 DOI: 10.1016/bs.mie.2019.11.009
Source DB: PubMed Journal: Methods Enzymol ISSN: 0076-6879 Impact factor: 1.600