| Literature DB >> 29058771 |
Hideaki Yano1, Marta Sánchez-Soto1, Sergi Ferré1.
Abstract
G protein-coupled receptors (GPCRs) comprise the single most targeted protein class in pharmacology. G protein signaling transduces extracellular stimuli such as neurotransmitters into cellular responses. Although preference for a specific GPCR among different G protein families (e.g., Gs-, Gi-, or Gq-like proteins) is often well studied, preference for a specific G protein subtype (e.g., Gi1, Gi2, Gi3, Go1, and Go2) has received little attention. Due to tissue expression differences and potentially exploitable functional differences, G protein subtype-dependent functional selectivity is an attractive framework to expand GPCR drug development. Herein we present a bioluminescence resonance energy transfer (BRET)-based method to characterize functional selectivity among Gi-like protein subtypes. © 2017 by John Wiley & Sons, Inc.Entities:
Keywords: BRET; G protein subtype; GPCR; catecholamine; functional selectivity
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Year: 2017 PMID: 29058771 PMCID: PMC5657550 DOI: 10.1002/cpns.38
Source DB: PubMed Journal: Curr Protoc Neurosci ISSN: 1934-8576