The complexity of G-protein coupled receptor-ligand interactions

被引:2
|
作者
Wang Ting [1 ]
机构
[1] Univ Calif Davis, Genome Ctr, Davis, CA 95616 USA
基金
美国国家卫生研究院;
关键词
G-protein coupled receptors (GPCR); ligand; interaction; functional selectivity; receptor subtype; SUBTYPE-SELECTIVE AGONISTS; 2ND EXTRACELLULAR LOOP; HIGH-AFFINITY BINDING; BETA(2)-ADRENERGIC RECEPTOR; ORPHAN GPCRS; CRYSTAL-STRUCTURE; DRUG DISCOVERY; MELANOCORTIN RECEPTORS; CONFORMATIONAL-CHANGES; MOLECULAR-MECHANISMS;
D O I
10.1007/s11426-013-4911-z
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The G-protein coupled receptors (GPCRs) play fundamental roles in the human biololgy and drug discovery. GPCRs function as signalling molecules that transduce extracellular signals into cells. The signalling transduction is generally triggered by interacting with ligands, including photons, ions, small organic compounds, peptides, proteins and lipids. In this review, we focus on interactions with diffusible ligands such as hormones and neurotransmitters. We discuss three aspects of the complexity of the GPCR-ligand interactions: functional selectivity of ligands, receptor subtype selectivity of ligands and orphan GPCRs.
引用
收藏
页码:1344 / 1350
页数:7
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