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钙离子介导的突触融合蛋白触发的胞吐作用的分子机制。

A molecular mechanism for calcium-mediated synaptotagmin-triggered exocytosis.

机构信息

Center for Membrane and Cell Physiology, University of Virginia, Charlottesville, VA, USA.

Department of Molecular Physiology and Biological Physics, University of Virginia, Charlottesville, VA, USA.

出版信息

Nat Struct Mol Biol. 2018 Oct;25(10):911-917. doi: 10.1038/s41594-018-0130-9. Epub 2018 Oct 5.

Abstract

The regulated exocytotic release of neurotransmitter and hormones is accomplished by a complex protein machinery whose core consists of SNARE proteins and the calcium sensor synaptotagmin-1. We propose a mechanism in which the lipid membrane is intimately involved in coupling calcium sensing to release. We found that fusion of dense core vesicles, derived from rat PC12 cells, was strongly linked to the angle between the cytoplasmic domain of the SNARE complex and the plane of the target membrane. We propose that, as this tilt angle increases, force is exerted on the SNARE transmembrane domains to drive the merger of the two bilayers. The tilt angle markedly increased following calcium-mediated binding of synaptotagmin to membranes, strongly depended on the surface electrostatics of the membrane, and was strictly coupled to the lipid order of the target membrane.

摘要

受调控的神经递质和激素的胞吐释放是由一个复杂的蛋白质机器完成的,其核心由 SNARE 蛋白和钙传感器突触结合蛋白-1 组成。我们提出了一种机制,其中脂质膜密切参与将钙感应与释放偶联。我们发现,源自大鼠 PC12 细胞的致密核心囊泡的融合与 SNARE 复合物的细胞质结构域与靶膜平面之间的夹角强烈相关。我们提出,随着这个倾斜角度的增加,力作用在 SNARE 跨膜结构域上,以驱动两个双层膜的融合。钙介导的突触结合蛋白与膜结合后,倾斜角度显著增加,强烈依赖于膜的表面静电,并且与靶膜的脂质有序性严格耦合。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ba3/6176490/1e5c61281423/nihms-1502306-f0001.jpg

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