From purified GPCRs to drug discovery: the promise of protein-based methodologies

被引:23
作者
Alkhalfioui, Fatima [1 ]
Magnin, Thierry [1 ]
Wagner, Renaud [1 ]
机构
[1] IREBS, F-67412 Illkirch Graffenstaden, France
关键词
RESONANCE ENERGY-TRANSFER; WAVE-GUIDE RESONANCE; X-RAY-STRUCTURE; COUPLED-RECEPTOR; CRYSTAL-STRUCTURE; BETA(2)-ADRENERGIC RECEPTOR; BIOSENSOR TECHNOLOGY; EXPRESSION SYSTEMS; MEMBRANE-PROTEINS; SQUID RHODOPSIN;
D O I
10.1016/j.coph.2009.04.002
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
G-protein-coupled receptors (GPCRs), the largest family of membrane proteins, represent ideal therapeutic targets for a number of disorders and diseases. Besides cell-based assays and high throughput screening (HTS), and thanks to the availability of milligram quantities of active purified receptors, protein-based approaches focusing on soluble GPCRs are growingly being used in this drug discovery effort. Along with the exploitation of GPCRs structures, innovative biochemical and biophysical approaches open up new routes for improving the knowledge of structure-activity relationships, for the identification of novel interacting partners and for the determination of receptor behaviour in different model environments. This review summarizes the state-of-the-art methodologies that robustly allow for the production and purification of soluble and active GPCRs, as well as the main outcomes that have been recently gained in GPCR biology using a panel of such protein-based approaches.
引用
收藏
页码:629 / 635
页数:7
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