α-突触核蛋白诱导的小单层囊泡变形。

Q3 Biochemistry, Genetics and Molecular Biology
QRB Discovery Pub Date : 2022-01-01 DOI:10.1017/qrd.2022.9
Katarzyna Makasewicz, Stefan Wennmalm, Sara Linse, Emma Sparr
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引用次数: 3

摘要

α-突触核蛋白是一种与脂质膜可逆结合的小神经元蛋白。膜的相互作用被认为是该蛋白健康功能的核心,参与突触可塑性和神经递质释放。α-Synuclein被推测可以诱导囊泡融合和裂变,这两个过程彼此相似,但进行方向不同,涉及不同的驱动力。本文从热力学的角度分析了α-突触核蛋白诱导的小单层囊泡变形。我们表明,在文献中解释为融合中间体的结构实际上是一种稳定的变形状态,既不会发生融合也不会发生囊泡聚集。我们推测了观察到的变形的驱动力,并提出了α-突触核蛋白在脂膜上的自组装先于并诱导了膜重构的假设。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

<i>α</i>-Synuclein-induced deformation of small unilamellar vesicles.

<i>α</i>-Synuclein-induced deformation of small unilamellar vesicles.

<i>α</i>-Synuclein-induced deformation of small unilamellar vesicles.

α-Synuclein-induced deformation of small unilamellar vesicles.

α-Synuclein is a small neuronal protein that reversibly associates with lipid membranes. The membrane interactions are believed to be central to the healthy function of this protein involved in synaptic plasticity and neurotransmitter release. α-Synuclein has been speculated to induce vesicle fusion as well as fission, processes which are analogous to each other but proceed in different directions and involve different driving forces. In the current work, we analyse α-synuclein-induced small unilamellar vesicle deformation from a thermodynamics point of view. We show that the structures interpreted in the literature as fusion intermediates are in fact a stable deformed state and neither fusion nor vesicle clustering occurs. We speculate on the driving force for the observed deformation and put forward a hypothesis that α-synuclein self-assembly on the lipid membrane precedes and induces membrane remodelling.

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来源期刊
QRB Discovery
QRB Discovery Biochemistry, Genetics and Molecular Biology-Biophysics
CiteScore
3.60
自引率
0.00%
发文量
18
审稿时长
12 weeks
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