代谢型谷氨酸受体
代谢型谷氨酸受体2
神经科学
机制(生物学)
代谢型谷氨酸受体5
变构调节
谷氨酸受体
代谢型谷氨酸受体7
代谢型谷氨酸受体6
C级GPCR
代谢型谷氨酸受体1
生物
化学
受体
生物化学
物理
量子力学
作者
Philippe Rondard,Jean‐Philippe Pin
标识
DOI:10.1016/j.coph.2014.12.001
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.
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