Nanobiology Institute and Department of Cell Biology, Yale University, New Haven, CT, USA.
Laboratoire de Physique de l'Ecole Normale Supérieure, ENS, Université PSL, CNRS, Sorbonne Université, Université Paris Cité, Paris, France.
FEBS Lett. 2023 Sep;597(18):2233-2249. doi: 10.1002/1873-3468.14718. Epub 2023 Sep 7.
Evidence from biochemistry, genetics, and electron microscopy strongly supports the idea that a ring of Synaptotagmin is central to the clamping and release of synaptic vesicles (SVs) for synchronous neurotransmission. Recent direct measurements in cell-free systems suggest there are 12 SNAREpins in each ready-release vesicle, consisting of six peripheral and six central SNAREpins. The six central SNAREpins are directly bound to the Synaptotagmin ring, are directly released by Ca , and they initially open the fusion pore. The six peripheral SNAREpins are indirectly bound to the ring, each linked to a central SNAREpin by a bridging molecule of Complexin. We suggest that the primary role of peripheral SNAREpins is to provide additional force to 'turbocharge' neurotransmitter release, explaining how it can occur much faster than other forms of membrane fusion. The SV protein Synaptophysin forms hexamers that bear two copies of the v-SNARE VAMP at each vertex, one likely assembling into a peripheral SNAREpin and the other into a central SNAREpin.
生物化学、遗传学和电子显微镜的证据有力地支持了这样一种观点,即突触融合蛋白的环是同步神经递质释放中突触小泡(SVs)夹闭和释放的核心。最近在无细胞系统中的直接测量表明,每个准备释放的囊泡中都有 12 个 SNAREpins,由六个外周和六个中央 SNAREpins 组成。六个中央 SNAREpins 直接与突触融合蛋白环结合,被 Ca 直接释放,它们最初打开融合孔。六个外周 SNAREpins 与环间接结合,每个 SNAREpins 通过复合蛋白的桥连分子与一个中央 SNAREpin 相连。我们认为,外周 SNAREpins 的主要作用是提供额外的力量来“涡轮增压”神经递质释放,解释了为什么它可以比其他形式的膜融合发生得更快。SV 蛋白突触小泡蛋白形成六聚体,每个顶点都有两个 v-SNARE VAMP 的拷贝,一个可能组装成外周 SNAREpins,另一个组装成中央 SNAREpins。