共 45 条
Restructuring G-Protein-Coupled Receptor Activation
被引:220
作者:

Audet, Martin
论文数: 0 引用数: 0
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机构:
Univ Montreal, Dept Biochem, Inst Res Immunol & Canc, Montreal, PQ H3C 3J7, Canada Univ Montreal, Dept Biochem, Inst Res Immunol & Canc, Montreal, PQ H3C 3J7, Canada

Bouvier, Michel
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Montreal, Dept Biochem, Inst Res Immunol & Canc, Montreal, PQ H3C 3J7, Canada Univ Montreal, Dept Biochem, Inst Res Immunol & Canc, Montreal, PQ H3C 3J7, Canada
机构:
[1] Univ Montreal, Dept Biochem, Inst Res Immunol & Canc, Montreal, PQ H3C 3J7, Canada
来源:
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.
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页码:14 / 23
页数:10
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