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首页> 外文期刊>Nature cell biology >Real-time measurements of vesicle-SNARE recycling in synapses of the central nervous system.
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Real-time measurements of vesicle-SNARE recycling in synapses of the central nervous system.

机译:实时测量中枢神经系统突触中囊泡-SNARE的循环。

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摘要

Following the fusion of synaptic vesicles with the presynaptic plasma membrane of nerve terminals by the process of exocytosis, synaptic-vesicle components are recycled to replenish the vesicle pool. Here we use a pH-sensitive green fluorescent protein to measure the residence time of VAMP, a vesicle-associated SNARE protein important for membrane fusion, on the surfaces of synaptic terminals of hippocampal neurons following exocytosis. The time course of VAMP retrieval depends linearly on the amount of VAMP that is added to the plasma membrane, with retrieval occurring between about 4 seconds and 90 seconds after exocytosis, and newly internalized vesicles are rapidly acidified. These data are well described by a model in which endocytosis appears to be saturable, but proceeds with an initial maximum velocity of about one vesicle per second. We also find that, following exocytosis, a portion of the newly inserted VAMP appears on the surface of the axon.
机译:在通过胞吐作用使突触小泡与神经末梢的突触前质膜融合之后,将突触小泡成分再循环以补充小泡池。在这里,我们使用pH敏感的绿色荧光蛋白来测量VAMP(胞外结合后海马神经元突触末端表面上对膜融合非常重要的囊泡相关SNARE蛋白)的停留时间。 VAMP回收的时间过程线性依赖于添加到质膜上的VAMP的量,回收发生在胞吐作用后约4秒至90秒之间,新内在化的囊泡会迅速酸化。这些数据被模型很好地描述,其中内吞作用似乎是饱和的,但是以大约每秒一个囊泡的初始最大速度进行。我们还发现,胞吐作用后,新插入的VAMP的一部分出现在轴突的表面。

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