Scaffold remodeling in space and time controls synaptic transmission.

Bioarchitecture Pub Date : 2012-02-01 DOI:10.4161/bioa.20381
Julie Perroy, Enora Moutin
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引用次数: 1

Abstract

Scaffolding proteins that are associated with glutamate receptors in dendritic spines govern the location and function of receptors to control synaptic transmission. Unraveling the spatio-temporal dynamics of protein-protein interactions within components of the scaffolding complex will bring to light the function of these interactions. Combining bioluminescence resonance energy transfer (BRET) imaging to electrophysiological recordings, we have recently shown that GKAP, a core protein of the scaffolding complex, interacts with DLC2, a protein associated with molecular motors. Synaptic activity-induced GKAP-DLC2 interaction in spines stabilizes the scaffolding complex and enhances the NMDA currents. Interestingly, this work placed emphasis on the bioarchitectural dependence of protein-protein interaction dynamics. Depending on physiological conditions, the modulation in space and time of protein-protein interaction is acutely regulated, engendering a subtle control of synaptic transmission in the state of the individual synapse.

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支架重构在空间和时间上控制突触传递。
树突棘中与谷氨酸受体相关的支架蛋白控制受体的位置和功能以控制突触传递。揭示脚手架复合体组件内蛋白质-蛋白质相互作用的时空动态将揭示这些相互作用的功能。结合生物发光共振能量转移(BRET)成像和电生理记录,我们最近发现GKAP是脚手架复合体的核心蛋白,与DLC2相互作用,DLC2是与分子马达相关的蛋白。突触活动诱导的脊髓中GKAP-DLC2相互作用稳定了支架复合物并增强了NMDA电流。有趣的是,这项工作强调了蛋白质-蛋白质相互作用动力学的生物建筑依赖性。根据生理条件,蛋白质-蛋白质相互作用在空间和时间上的调节受到强烈调节,从而在单个突触状态下对突触传递产生微妙的控制。
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