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α-突触核蛋白的膜相互作用

The Membrane Interaction of Alpha-Synuclein.

作者信息

Liu Cencen, Zhao Yunfei, Xi Huan, Jiang Jie, Yu Yang, Dong Wei

机构信息

Key Laboratory of Medical Electrophysiology of Ministry of Education and Medical Electrophysiological Key Laboratory of Sichuan Province, Institute of Cardiovascular Research, Southwest Medical University, Luzhou, China.

Department of Histology and Embryology, School of Basic Medical Sciences, Southwest Medical University, Luzhou, China.

出版信息

Front Cell Neurosci. 2021 Mar 4;15:633727. doi: 10.3389/fncel.2021.633727. eCollection 2021.

Abstract

A presynaptic protein closely related to Parkinson's disease (PD), α-synuclein (α-Syn), has been studied extensively regarding its pathogenic mechanisms. As a physiological protein in presynapses, however, α-Syn's physiological function remains unclear. Its location in nerve terminals and effects on membrane fusion also imply its functional role in synaptic transmission, including its possible interaction with high-curvature membranes its N-terminus and amorphous C-terminus. PD-related mutants that disrupt the membrane interaction (e.g., A30P and G51D) additionally suggest a relationship between α-Syn's pathogenic mechanisms and physiological roles through the membrane binding. Here, we summarize recent research on how α-Syn and its variants interact with membranes and influence synaptic transmission. We list several membrane-related connections between the protein's physiological function and the pathological mechanisms that stand to expand current understandings of α-Syn.

摘要

一种与帕金森病(PD)密切相关的突触前蛋白α-突触核蛋白(α-Syn),其致病机制已得到广泛研究。然而,作为突触前的一种生理蛋白,α-Syn的生理功能仍不清楚。它在神经末梢的定位以及对膜融合的影响也暗示了其在突触传递中的功能作用,包括其N端和无定形C端与高曲率膜的可能相互作用。破坏膜相互作用的帕金森病相关突变体(如A30P和G51D)进一步表明,通过膜结合,α-Syn的致病机制与生理作用之间存在关联。在这里,我们总结了关于α-Syn及其变体如何与膜相互作用并影响突触传递的最新研究。我们列出了该蛋白生理功能与病理机制之间的几种与膜相关的联系,这些联系有望扩展目前对α-Syn的理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6c0/7969880/c7fa1334ef61/fncel-15-633727-g0001.jpg

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