Mahal Lara K, Sequeira Sonia M, Gureasko Jodi M, Söllner Thomas H
Cellular Biochemistry and Biophysics Program, Memorial Sloan Kettering Cancer Center, 1275 York Avenue, New York, NY 10021, USA.
J Cell Biol. 2002 Jul 22;158(2):273-82. doi: 10.1083/jcb.200203135. Epub 2002 Jul 15.
Neurotransmitter release requires the direct coupling of the calcium sensor with the machinery for membrane fusion. SNARE proteins comprise the minimal fusion machinery, and synaptotagmin I, a synaptic vesicle protein, is the primary candidate for the main neuronal calcium sensor. To test the effect of synaptotagmin I on membrane fusion, we incorporated it into a SNARE-mediated liposome fusion assay. Synaptotagmin I dramatically stimulated membrane fusion by facilitating SNAREpin zippering. This stimulatory effect was topologically restricted to v-SNARE vesicles (containing VAMP 2) and only occurred in trans to t-SNARE vesicles (containing syntaxin 1A and SNAP-25). Interestingly, calcium did not affect the overall fusion reaction. These results indicate that synaptotagmin I can directly accelerate SNARE-mediated membrane fusion and raise the possibility that additional components might be required to ensure tight calcium coupling.
神经递质释放需要钙传感器与膜融合机制直接偶联。SNARE蛋白构成了最小的融合机制,而突触结合蛋白I(一种突触小泡蛋白)是主要神经元钙传感器的主要候选者。为了测试突触结合蛋白I对膜融合的影响,我们将其纳入SNARE介导的脂质体融合试验中。突触结合蛋白I通过促进SNAREpin拉链化显著刺激了膜融合。这种刺激作用在拓扑结构上仅限于v-SNARE囊泡(含有VAMP 2),并且仅在与t-SNARE囊泡(含有 syntaxin 1A和SNAP-25)反式作用时发生。有趣的是,钙并不影响整体融合反应。这些结果表明,突触结合蛋白I可以直接加速SNARE介导的膜融合,并增加了可能需要其他成分来确保紧密钙偶联的可能性。