Davis A F, Bai J, Fasshauer D, Wolowick M J, Lewis J L, Chapman E R
Department of Physiology, University of Wisconsin School of Medicine, Madison 53706, USA.
Neuron. 1999 Oct;24(2):363-76. doi: 10.1016/s0896-6273(00)80850-8.
The synaptic vesicle protein synaptotagmin I binds Ca2+ and is required for efficient neurotransmitter release. Here, we measure the response time of the C2 domains of synaptotagmin to determine whether synaptotagmin is fast enough to function as a Ca2+ sensor for rapid exocytosis. We report that synaptotagmin is "tuned" to sense Ca2+ concentrations that trigger neuronal exocytosis. The speed of response is unique to synaptotagmin I and readily satisfies the kinetic constraints of synaptic vesicle membrane fusion. We further demonstrate that Ca2+ triggers penetration of synaptotagmin into membranes and simultaneously drives assembly of synaptotagmin onto the base of the ternary SNARE (soluble N-ethylmaleimide-sensitive fusion protein [NSF] attachment receptor) complex, near the transmembrane anchor of syntaxin. These data support a molecular model in which synaptotagmin triggers exocytosis through its interactions with membranes and the SNARE complex.
突触囊泡蛋白突触结合蛋白I能结合Ca2+,是高效神经递质释放所必需的。在此,我们测量突触结合蛋白C2结构域的响应时间,以确定突触结合蛋白是否足够快速,能够作为快速胞吐作用的Ca2+传感器发挥作用。我们报告称,突触结合蛋白经过“调整”,可感知触发神经元胞吐作用的Ca2+浓度。响应速度是突触结合蛋白I所特有的,很容易满足突触囊泡膜融合的动力学限制。我们进一步证明,Ca2+触发突触结合蛋白穿透膜,并同时驱动突触结合蛋白在三元SNARE(可溶性N-乙基马来酰亚胺敏感融合蛋白[NSF]附着受体)复合物基部组装,靠近Syntaxin的跨膜锚定部位。这些数据支持了一个分子模型,即突触结合蛋白通过与膜和SNARE复合物的相互作用触发胞吐作用。