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兴奋性突触处谷氨酸受体聚集的分子机制。

Molecular mechanisms of glutamate receptor clustering at excitatory synapses.

作者信息

O'Brien R J, Lau L F, Huganir R L

机构信息

Howard Hughes Medical Institute, Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, USA.

出版信息

Curr Opin Neurobiol. 1998 Jun;8(3):364-9. doi: 10.1016/s0959-4388(98)80062-7.

Abstract

The targeting of AMPA- and NMDA-type glutamate receptors to synapses in the central nervous system is essential for efficient excitatory synaptic transmission. Recent studies have indicated that protein-protein interactions of these receptors with synaptic proteins that contain PDZ domains are crucial for receptor targeting. NMDA receptors have been found to bind to the PSD-95 family of proteins, whereas AMPA receptors interact with the PDZ-domain-containing protein GRIP (glutamate receptor interacting protein). PSD-95 and GRIP contain multiple PDZ domains as well as other protein-protein interaction motifs that help to form large macromolecular complexes that may be important for the formation and plasticity of synapses.

摘要

将AMPA型和NMDA型谷氨酸受体靶向至中枢神经系统的突触对于高效的兴奋性突触传递至关重要。最近的研究表明,这些受体与含有PDZ结构域的突触蛋白之间的蛋白质-蛋白质相互作用对于受体靶向至关重要。已发现NMDA受体与PSD-95家族蛋白结合,而AMPA受体与含PDZ结构域的蛋白GRIP(谷氨酸受体相互作用蛋白)相互作用。PSD-95和GRIP含有多个PDZ结构域以及其他蛋白质-蛋白质相互作用基序,这些基序有助于形成大型大分子复合物,这可能对突触的形成和可塑性很重要。

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