THE FAMILY OF G-PROTEIN-COUPLED RECEPTORS

被引:320
作者
STRADER, CD
FONG, TM
GRAZIANO, MP
TOTA, MR
机构
[1] Molec. Pharmacol./Biochemistry Dept., Merck Research Laboratories, Box 2000, Rahway
关键词
AMINO ACID SEQUENCES; PEPTIDE BINDING SITE; SIGNAL TRANSDUCTION; MUTAGENESIS; HELICES;
D O I
10.1096/fasebj.9.9.7601339
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
The family of G-protein-coupled receptors can be defined by their similar structural and functional characteristics. Although their primary sequences are quite diverse, these proteins share several common structural features that reflect their common mechanism of action. Mutagenesis and biophysical analysis of several of these receptors indicate that small molecule agonists and antagonists bind to a hydrophobic pocket buried in the transmembrane core of the receptor. In contrast, peptide ligands bind to both the extracellular and transmembrane domains. The mechanisms by which these peptide and small molecule agonists cause receptor activation are being explored by various approaches, but are not yet well defined. A deeper understanding of structural basis for the functional activity of this large family of receptors will have important implications for drug design in a variety of therapeutic areas.
引用
收藏
页码:745 / 754
页数:10
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