Muscarinic acetylcholine receptors: novel opportunities for drug development

被引:325
作者
Kruse, Andrew C. [1 ]
Kobilka, Brian K. [1 ]
Gautam, Dinesh [2 ]
Sexton, Patrick M. [3 ,4 ]
Christopoulos, Arthur [3 ,4 ]
Wess, Juergen [2 ]
机构
[1] Stanford Univ, Sch Med, Dept Mol & Cellular Physiol, Stanford, CA 94305 USA
[2] NIDDK, Mol Signaling Sect, Bioorgan Chem Lab, US Natl Inst Hlth, Bethesda, MD 20892 USA
[3] Monash Univ, Monash Inst Pharmaceut Sci, Parkville, Vic 3052, Australia
[4] Monash Univ, Dept Pharmacol, Parkville, Vic 3052, Australia
基金
澳大利亚国家健康与医学研究理事会; 英国医学研究理事会; 美国国家科学基金会;
关键词
PROTEIN-COUPLED RECEPTORS; 2ND ALLOSTERIC SITE; CRYSTAL-STRUCTURE; FUNCTIONAL SELECTIVITY; BITOPIC LIGANDS; PROBE-DEPENDENCE; STRUCTURAL BASIS; INSULIN-RELEASE; BINDING-SITES; M-1; RECEPTOR;
D O I
10.1038/nrd4295
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The muscarinic acetylcholine receptors are a subfamily of G protein-coupled receptors that regulate numerous fundamental functions of the central and peripheral nervous system. The past few years have witnessed unprecedented new insights into muscarinic receptor physiology, pharmacology and structure. These advances include the first structural views of muscarinic receptors in both inactive and active conformations, as well as a better understanding of the molecular underpinnings of muscarinic receptor regulation by allosteric modulators. These recent findings should facilitate the development of new muscarinic receptor subtype-selective ligands that could prove to be useful for the treatment of many severe pathophysiological conditions.
引用
收藏
页码:549 / 560
页数:12
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