Endocytosis of the synaptic vesicle protein, synaptophysin, requires the COOH-terminal tail.

Journal de physiologie Pub Date : 1991-01-01
A D Linstedt, R B Kelly
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引用次数: 0

Abstract

Synaptic vesicles participate in a cycle of fusion with the plasma membrane and reformation by endocytosis. Endocytosis of membrane proteins by the well studied clathrin-coated vesicle pathway has been shown to involve specific sequences within the cytoplasmic tail domain. Proteins taken up by clathrin-coated vesicles are directed to early endosomes from which they may return to plasma membrane. Recent evidence suggests that the synaptic vesicle protein synaptophysin is targeted to early endosomes in transfected fibroblasts and in neuroendocrine cells. To begin to test whether sequences within the COOH-cytoplasmic domain are required for internalization we have expressed a synaptophysin molecule lacking this domain in 3T3 cells and measured its rate of internalization. While a full length synaptophysin was internalized efficiently, we could not detect internalization of the mutant construct. These data are consistent with a model in which the COOH-terminal tail is required for coated-pit localization and hence targeting of synaptophysin to early endosomes.

突触泡蛋白(synaptophysin)的内吞作用需要cooh末端的尾部。
突触囊泡参与与质膜融合和内吞作用重组的循环。研究表明,通过网格蛋白包覆的囊泡途径,膜蛋白的内吞作用涉及细胞质尾部区域内的特定序列。被网格蛋白包裹的小泡吸收的蛋白质被引导到早期的核内体,它们可能从核内体返回到质膜。最近的证据表明突触囊泡蛋白synaptophysin在转染的成纤维细胞和神经内分泌细胞中靶向早期内体。为了开始测试cooh -细胞质结构域内的序列是否需要内化,我们在3T3细胞中表达了一个缺乏该结构域的突触素分子,并测量了其内化率。虽然全长synaptophysin被有效内化,但我们无法检测到突变结构的内化。这些数据与一个模型是一致的,在这个模型中,cooh末端尾巴是涂层坑定位所必需的,因此突触体素的目标是早期核内体。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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