Restructuring G-Protein-Coupled Receptor Activation

被引:220
作者
Audet, Martin [1 ]
Bouvier, Michel [1 ]
机构
[1] Univ Montreal, Dept Biochem, Inst Res Immunol & Canc, Montreal, PQ H3C 3J7, Canada
关键词
BETA(2) ADRENERGIC-RECEPTOR; MUSCARINIC ACETYLCHOLINE-RECEPTOR; ADENOSINE A(2A) RECEPTOR; LIPIDIC CUBIC PHASES; CRYSTAL-STRUCTURE; OPIOID RECEPTOR; BETA(1)-ADRENERGIC RECEPTOR; MEMBRANE-PROTEINS; ANTAGONIST; COMPLEX;
D O I
10.1016/j.cell.2012.09.003
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
G-protein-coupled receptors serve as key signal transduction conduits, linking extracellular inputs with diverse cellular responses. These receptors eluded structural characterization for decades following their identification. A landmark structure of rhodopsin provided a basis for structure-function studies and homology modeling, but advances in receptor biology suffered from a lack of receptor-specific structural insights. The recent explosion in GPCR structures confirms some features predicted by rhodopsin-based models, and more importantly, it reveals unexpected ligand-binding modes and critical aspects of the receptor activation process. The new structures also promise to foster studies testing emerging models for GPCR function such as receptor dimerization and ligand-biased signaling.
引用
收藏
页码:14 / 23
页数:10
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