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突触结合蛋白I对膜融合和SNAREpin形成的钙非依赖性刺激。

Calcium-independent stimulation of membrane fusion and SNAREpin formation by synaptotagmin I.

作者信息

Mahal Lara K, Sequeira Sonia M, Gureasko Jodi M, Söllner Thomas H

机构信息

Cellular Biochemistry and Biophysics Program, Memorial Sloan Kettering Cancer Center, 1275 York Avenue, New York, NY 10021, USA.

出版信息

J Cell Biol. 2002 Jul 22;158(2):273-82. doi: 10.1083/jcb.200203135. Epub 2002 Jul 15.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/56da/2173117/f86907cca5a5/200203135f1a.jpg

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