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突触小泡内体供体区室包被机制的生化特性

Biochemical characterization of the coating mechanism of the endosomal donor compartment of synaptic vesicles.

作者信息

Horng Jim-Tong, Tan Chung-Yueh

机构信息

Department of Biochemistry, Chang Gung University, Kweishan, Taiwan.

出版信息

Neurochem Res. 2004 Jul;29(7):1411-6. doi: 10.1023/b:nere.0000026405.62006.88.

Abstract

The heterotetrameric adaptor protein complex, AP-3, sorts proteins to both the endosome/lysosome and the synaptic vesicles. We have characterized the recruitment of pure AP-3 complex and ADP-ribosylation factor (ARF) onto the endosomal donor compartments that give rise to synaptic vesicles. We demonstrated that endosomes become heavier in a sucrose gradient after incubation with rat brain cytosol and a nonhydrolyzable GTP analog, GTPgammaS. This process requires a small GTPase, ARF-1. Furthermore, the endosomal coating is specific for AP-3 but not the AP-2 complex. This process requires only two soluble proteins AP-3 and ARF, with the recruitment of AP-3 being saturable at about 30 nM. These results establish that the synaptic vesicle's donor membrane is coated with AP-3 before vesiculation, in a coat-protein-specific and dose-dependent fashion.

摘要

异源四聚体衔接蛋白复合物AP-3可将蛋白质分选至内体/溶酶体以及突触小泡。我们已经对纯AP-3复合物和ADP核糖基化因子(ARF)募集到产生突触小泡的内体供体区室进行了表征。我们证明,用大鼠脑细胞质溶胶和不可水解的GTP类似物GTPγS孵育后,内体在蔗糖梯度中会变重。这个过程需要一种小GTP酶ARF-1。此外,内体包被对AP-3具有特异性,而对AP-2复合物则没有。这个过程仅需要两种可溶性蛋白AP-3和ARF,AP-3的募集在约30 nM时达到饱和。这些结果表明,突触小泡的供体膜在出泡之前以一种衣被蛋白特异性和剂量依赖性的方式被AP-3包被。

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