Rondard Philippe, Pin Jean-Philippe
CNRS, UMR5203, Institut de Génomique Fonctionnelle, Montpellier, France; INSERM, U661, Montpellier, France; Université Montpellier 1 & 2, Montpellier F-34000, France.
CNRS, UMR5203, Institut de Génomique Fonctionnelle, Montpellier, France; INSERM, U661, Montpellier, France; Université Montpellier 1 & 2, Montpellier F-34000, France.
Curr Opin Pharmacol. 2015 Feb;20:95-101. doi: 10.1016/j.coph.2014.12.001. Epub 2014 Dec 17.
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.
代谢型谷氨酸受体(mGluRs)是谷氨酸激活的G蛋白偶联受体,在中枢神经系统中广泛表达。8种mGluRs亚型调节许多突触处的传递,是治疗多种神经和精神疾病的有趣治疗靶点。特别是,它们在多个结构域和亚基中的组织为开发以不同效力调节mGluRs活性的药物提供了各种可能性。最近的结构、生物物理和功能分析为mGluR激活和动力学机制提供了新的见解。它们还揭示了配体效力的结构基础,从而提供了部分激动剂和变构调节剂的可能作用机制。这些新发现对于开发新型mGluR亚型选择性化合物具有重要意义。