| Literature DB >> 33985815 |
Haitao Zhang1, Aleksandra Luginina2, Alexey Mishin2, Mithu Baidya3, Arun K Shukla4, Vadim Cherezov5.
Abstract
G protein-coupled angiotensin II receptors, AT1R and AT2R, are integral components of the renin-angiotensin system (RAS) that regulates blood pressure and fluid balance in humans. While AT1R is a well-established target of angiotensin receptor blockers (ARBs) for managing hypertension and a prime system for studying biased signaling, AT2R has been recognized as a promising target against neuropathic pain and lung fibrosis. In this review, we discuss how recent structural advances illuminate ligand-binding modes and subtype selectivity, shared and distinct features of the receptors, their transducer-coupling patterns, and downstream signaling responses. We also underscore the key ATR aspects that require further studies to fully appreciate the mechanistic framework that fine-tunes their cellular and physiological functions, providing untapped potential for drug discovery.Entities:
Keywords: G protein-coupled receptors; activation mechanism; angiotensin II receptors; biased signaling; ligand; subtype selectivity
Mesh:
Substances:
Year: 2021 PMID: 33985815 PMCID: PMC7611150 DOI: 10.1016/j.tips.2021.04.006
Source DB: PubMed Journal: Trends Pharmacol Sci ISSN: 0165-6147 Impact factor: 14.819