Dynamics and modulation of metabotropic glutamate receptors

被引:45
作者
Rondard, Philippe [1 ,2 ,3 ,4 ]
Pin, Jean-Philippe [1 ,2 ,3 ,4 ]
机构
[1] CNRS, UMR5203, Inst Genom Fonct, Montpellier, France
[2] INSERM, Montpellier, France
[3] Univ Montpellier I, F-34000 Montpellier, France
[4] Univ Montpellier 2, F-34000 Montpellier, France
关键词
PROTEIN-COUPLED RECEPTORS; ALLOSTERIC MODULATORS; CRYSTAL-STRUCTURE; ACTIVATION MECHANISM; STRUCTURAL BASIS; OPIOID RECEPTOR; LIGAND-BINDING; CNS DISORDERS; GPCR; PHARMACOLOGY;
D O I
10.1016/j.coph.2014.12.001
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The metabotropic glutamate receptors (mGluRs) are glutamate-activated G protein-coupled receptors widely expressed in the central nervous system. The eight mGluRs subtypes modulate transmission at many synapses, and are interesting therapeutic targets for the treatment of many neurological and psychiatric diseases. In particular, their organization in multiple domains and subunits offers various possibilities for the development of drugs that modulate mGluRs activity with different efficacies. Recent structural, biophysical and functional analyses have provided new insights into the mechanism of mGluR activation and dynamics. They also revealed the structural bases of ligand efficacy then providing possible mechanism of action of partial agonists and allosteric modulators. These new findings are of great interest for the development of novel mGluR subtype-selective compounds.
引用
收藏
页码:95 / 101
页数:7
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