Discovery of New GPCR Biology: One Receptor Structure at a Time

被引:148
作者
Hanson, Michael A. [1 ]
Stevens, Raymond C. [1 ]
机构
[1] Scripps Res Inst, Dept Mol Biol, La Jolla, CA 92037 USA
关键词
PROTEIN-COUPLED RECEPTOR; CRYSTAL-STRUCTURE; MEMBRANE-PROTEINS; LACTOSE PERMEASE; SQUID RHODOPSIN; CRYSTALLIZATION; FORM; CHOLESTEROL; MESOPHASES; OPSIN;
D O I
10.1016/j.str.2008.12.003
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 (GPCRs) are the largest family of proteins in the human genome. Within the last year, we have witnessed a relative explosion in the amount of structural information available for the GPCR family with two new structures of opsin in the presence and absence of transducin peptide, four new structures of beta-adrenergic receptors, and a recent structure of the human adenosine A(2A) receptor. The new biological insight being gained, such as the highly divergent extracellular loops and areas of structural convergence within the transmembrane helices, allows us to chart a course for further investigation into this important class of membrane proteins.
引用
收藏
页码:8 / 14
页数:7
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