Han Jing, Pluhackova Kristyna, Böckmann Rainer A
Department of Biochemistry and Molecular Biology, School of Basic Medical Sciences, Xi'an Jiaotong University Health Science CenterXi'an, China; Computational Biology, Department of Biology, Friedrich-Alexander Universität Erlangen-NürnbergErlangen, Germany.
Computational Biology, Department of Biology, Friedrich-Alexander Universität Erlangen-Nürnberg Erlangen, Germany.
Front Physiol. 2017 Jan 20;8:5. doi: 10.3389/fphys.2017.00005. eCollection 2017.
Membrane fusion is a key process in all living organisms that contributes to a variety of biological processes including viral infection, cell fertilization, as well as intracellular transport, and neurotransmitter release. In particular, the various membrane-enclosed compartments in eukaryotic cells need to exchange their contents and communicate across membranes. Efficient and controllable fusion of biological membranes is known to be driven by cooperative action of SNARE proteins, which constitute the central components of the eukaryotic fusion machinery responsible for fusion of synaptic vesicles with the plasma membrane. During exocytosis, vesicle-associated v-SNARE (synaptobrevin) and target cell-associated t-SNAREs (syntaxin and SNAP-25) assemble into a core trans-SNARE complex. This complex plays a versatile role at various stages of exocytosis ranging from the priming to fusion pore formation and expansion, finally resulting in the release or exchange of the vesicle content. This review summarizes current knowledge on the intricate molecular mechanisms underlying exocytosis triggered and catalyzed by SNARE proteins. Particular attention is given to the function of the peptidic SNARE membrane anchors and the role of SNARE-lipid interactions in fusion. Moreover, the regulatory mechanisms by synaptic auxiliary proteins in SNARE-driven membrane fusion are briefly outlined.
膜融合是所有生物中的一个关键过程,它有助于多种生物过程,包括病毒感染、细胞受精以及细胞内运输和神经递质释放。特别是,真核细胞中各种膜封闭的区室需要交换它们的内容物并跨膜进行通信。已知生物膜的高效且可控的融合是由SNARE蛋白的协同作用驱动的,SNARE蛋白构成了负责突触小泡与质膜融合的真核融合机制的核心成分。在胞吐作用期间,囊泡相关的v-SNARE(突触小泡蛋白)和靶细胞相关的t-SNARE( syntaxin和SNAP-25)组装成一个核心反式SNARE复合体。该复合体在胞吐作用的各个阶段发挥着多种作用,从引发到融合孔的形成和扩张,最终导致囊泡内容物的释放或交换。本综述总结了目前关于由SNARE蛋白触发和催化的胞吐作用背后复杂分子机制的知识。特别关注肽类SNARE膜锚定物的功能以及SNARE-脂质相互作用在融合中的作用。此外,还简要概述了突触辅助蛋白在SNARE驱动的膜融合中的调节机制。