The G protein-coupled receptor N-terminus and receptor signalling: N-tering a new era

被引:37
作者
Coleman, James U. [1 ,2 ]
Ngo, Tony [1 ,2 ]
Smith, Nicola J. [1 ,2 ]
机构
[1] Victor Chang Cardiac Res Inst, Mol Pharmacol Grp, Darlinghurst, NSW 2010, Australia
[2] Univ New South Wales, St Vincents Clin Sch, Darlinghurst, NSW 2010, Australia
基金
英国医学研究理事会;
关键词
GPCR; G protein-coupled receptor; N-terminus; Proteolysis; Signalling; ENDOTHELIN-B-RECEPTOR; HUMAN THYROTROPIN RECEPTOR; CRYSTAL-STRUCTURE; THROMBIN RECEPTOR; INVERSE AGONIST; MELANOCORTIN-4; RECEPTOR; CONSTITUTIVE ACTIVITY; ACTIVATED RECEPTOR; MOLECULAR-CLONING; LINKED GLYCOSYLATION;
D O I
10.1016/j.cellsig.2017.02.004
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
G protein-coupled receptors (GPCRs) are a vast family of membrane-traversing proteins, essential to the ability of eukaryotic life to detect, and mount an intracellular response to, a diverse range of extracellular stimuli. GPCRs have evolved with archetypal features including an extracellular N-terminus and intracellular C-terminus that flank a transmembrane structure of seven sequential helices joined by intracellular and extracellular loops. These structural domains contribute to the ability of a GPCR to be correctly synthesised and inserted into the cell membrane, to interact with its cognate ligand(s) and to couple with signal-transducing heterotrimeric G proteins, allowing the activated receptor to selectively modulate a number of signalling cascades. Whilst well known for its importance in receptor translation and trafficking, the GPCR N-terminus is underexplored as a participant in receptor signalling. This review aims to discuss and integrate recent advances in knowledge of the vital roles of the GPCR N-terminus in receptor signalling. (C) 2017 Elsevier Inc. All rights reserved.
引用
收藏
页码:1 / 9
页数:9
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