Ramirez Denise M O, Kavalali Ege T
Cell Logist. 2012 Jan 1;2(1):20-27. doi: 10.4161/cl.20114.
An increasing number of studies suggest that distinct pools of synaptic vesicles drive specific forms of neurotransmission. Interspersed with these functional studies are analyses of the synaptic vesicle proteome which have consistently detected the presence of so-called "non-canonical" SNAREs that typically function in fusion and trafficking of other subcellular structures within the neuron. The recent identification of certain non-canonical vesicular SNAREs driving spontaneous (e.g., VAMP7 and vti1a) or evoked asynchronous (e.g., VAMP4) release integrates and corroborates existing data from functional and proteomic studies and implies that at least some complement of non-canonical SNAREs resident on synaptic vesicles function in neurotransmission. Here, we discuss the specific roles in neurotransmission of proteins homologous to each member of the classical neuronal SNARE complex consisting of synaptobrevin2, syntaxin-1, and SNAP-25.
越来越多的研究表明,不同的突触小泡池驱动着特定形式的神经传递。在这些功能研究的同时,也穿插着对突触小泡蛋白质组的分析,这些分析一直检测到所谓“非典型”SNARE蛋白的存在,它们通常在神经元内其他亚细胞结构的融合和运输中发挥作用。最近发现某些非典型囊泡SNARE蛋白驱动自发释放(如VAMP7和vti1a)或诱发的异步释放(如VAMP4),整合并证实了功能和蛋白质组学研究的现有数据,这意味着至少一些存在于突触小泡上的非典型SNARE蛋白在神经传递中发挥作用。在此,我们讨论与由突触融合蛋白2、 syntaxin-1和SNAP-25组成的经典神经元SNARE复合体的每个成员同源的蛋白质在神经传递中的具体作用。