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SNARE 复合物与膜的动态关系。

Dynamic Relationship of the SNARE Complex with a Membrane.

机构信息

Department of Pharmacology, University of Michigan Medical School, Ann Arbor, Michigan.

Division of Basic and Translational Biophysics, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland.

出版信息

Biophys J. 2019 Aug 20;117(4):627-630. doi: 10.1016/j.bpj.2019.07.010. Epub 2019 Jul 16.

Abstract

Fusion of secretory granules and synaptic vesicles with the plasma membrane is driven by SNARE protein interactions. Intensive investigations in vitro, which include x-ray crystallography, cryoelectron microscopy, and NMR analyses by numerous groups, have elucidated structures relevant to the function of these proteins. Although function depends on the proteins being membrane bound, for experimental reasons, most of the studies have used cytosolic domains, as exemplified by the groundbreaking studies that elucidated the structure of a tetrapeptide helical bundle formed by interaction of the cytosolic domains of syntaxin1A, SNAP25 (two peptides) and synaptobrevin 2. Because the cytosolic fragments were unfettered by membrane attachments, it is likely that the tetrapeptide helical bundle reflects the lowest energy state, such as that found in the "cis" interactions of the SNARE motifs after fusion when they co-localize in the plasma membrane. Much more difficult to study and still poorly understood are critical "trans" interactions between the synaptic vesicle SNARE protein synaptobrevin 2 and the plasma membrane syntaxin1A/SNAP25 complex that initiate the fusion event. In a series of articles from the laboratory of Lukas Tamm, the spontaneous orientation of the SNARE motif of membrane-bound, full-length syntaxin1A with respect to the membrane hosting syntaxin's transmembrane domain was investigated with nanometer precision under a variety of conditions, including those that model aspects of the "trans" configuration. The studies rely on fluorescence interference-contrast microscopy, a technique that utilizes the pattern of constructive and destructive interference arising from incoming and reflected excitation and emission light at the surface of a silicon chip that has been layered with oxidized silicon of varying depths. This Perspective discusses their findings, including the unexpected influence of the degree of lipid unsaturation on the orientation of the SNARE complex.

摘要

融合的分泌小泡和突触囊泡与质膜是由 SNARE 蛋白相互作用驱动的。在体外的深入研究,包括 X 射线晶体学、低温电子显微镜和 NMR 分析的许多团体,已经阐明了这些蛋白质的功能相关的结构。虽然功能取决于蛋白质被膜结合,由于实验的原因,大多数的研究都使用胞质域,作为例证的开创性的研究,阐明了由相互作用的胞质结构域组成的四肽螺旋束的结构 syntaxin1A、SNAP25(两个肽)和 synaptobrevin 2。因为胞质片段不受膜附着的束缚,所以四肽螺旋束很可能反映了最低的能量状态,例如在融合时 SNARE 基序的“顺式”相互作用中发现的那样,当它们在质膜中共定位时。更难以研究,仍然理解得很差的是突触囊泡 SNARE 蛋白 synaptobrevin 2 和质膜 syntaxin1A/SNAP25 复合物之间的关键“反式”相互作用,该相互作用启动融合事件。在卢卡斯·塔姆(Lukas Tamm)实验室的一系列文章中,用纳米精度研究了膜结合全长 syntaxin1A 的 SNARE 基序相对于含有 syntaxin 跨膜结构域的膜的自发取向,包括那些模拟“反式”构型的各个方面的条件。这些研究依赖于荧光干涉对比显微镜技术,该技术利用来自入射和反射激发和发射光的建设性和破坏性干涉的图案,在已经分层的氧化硅的不同深度的硅芯片表面上。这篇观点文章讨论了他们的发现,包括脂质不饱和程度对 SNARE 复合物取向的意外影响。

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Entropic forces drive self-organization and membrane fusion by SNARE proteins.熵力通过 SNARE 蛋白驱动自组织和膜融合。
Proc Natl Acad Sci U S A. 2017 May 23;114(21):5455-5460. doi: 10.1073/pnas.1611506114. Epub 2017 May 10.
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Role of the synaptobrevin C terminus in fusion pore formation.突触融合蛋白 C 端在融合孔形成中的作用。
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