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Mini-Reviews in Medicinal Chemistry

Editor-in-Chief

ISSN (Print): 1389-5575
ISSN (Online): 1875-5607

Biased Agonism of the Angiotensin II Type 1 Receptor

Author(s): C. M. Godin and S. S.G. Ferguson

Volume 12, Issue 9, 2012

Page: [812 - 816] Pages: 5

DOI: 10.2174/138955712800959134

Price: $65

Abstract

G protein-coupled receptors (GPCRs) can be activated by multiple ligands and exhibit the capacity to couple to numerous intracellular signal transduction pathways. This property allows GPCRs to be modulated by biased agonists that selectively activate specific subsets of GPCR-regulated cellular signaling proteins. The angiotensin II type 1 receptor (AT1R) is a GPCR that endogenously binds to the peptide ligand angiotensin II. More recently it has been demonstrated that a modified peptide, [Sar1I-le4-Ile8]-angiotensin II (SII) acts as a biased agonist towards the AT1R. SII binds to the AT1R without promoting heterotrimeric G protein-coupling, but serves to link the receptor to the beta-arrestin-dependent activation of the mitogen activated protein kinase pathway. The present mini-review summarizes current knowledge regarding the role of biased agonists in stimulating biased AT1R signaling.

Keywords: Angiotensin II, SII, biased agonism, GPCR, G-protein, phosphorylation, GRK6-dependent, Cardiovascular Disease, Mechanical Stretch, phosphoinositol-4


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