早期内吞Rabs:功能预测到功能表征。

Jeremy C Simpson, Arwyn T Jones
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引用次数: 33

摘要

内吞途径是分子进入细胞的高度动态通道。功能和特异性在一定程度上是由一些被称为Rabs的小gtp酶控制的。在特定的细胞位置,Rabs通过与细胞器膜和一系列影响因子和效应分子的特异性相互作用,介导膜运输的多种功能。在内吞途径中,Rabs已被证明可以控制质膜上囊泡的形成以及内化分子的下游传递到许多细胞位置。由于许多Rabs位于内吞途径上,内化分子在到达最终目的地的途中可能会穿过许多rabb特定的变电站或子域。Rabs 5、21和22都定位于早期内吞途径,并被证明具有许多共同的特征,值得将它们分离成一个单一的功能内吞基团。在这篇综述中,我们比较了描述内核体形态和功能的异同的实验,这些形态学和功能是由它们在细胞中的表达介导的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Early endocytic Rabs: functional prediction to functional characterization.

Endocytic pathways are highly dynamic gateways for molecules to enter cells. Functionality and specificity is in part controlled by a number of small GTPases called Rabs. In defined cellular locations, Rabs mediate multiple functions in membrane trafficking via their specific interaction with organelle membranes and a host of affector and effector molecules. On endocytic pathways, Rabs have been shown to control the formation of vesicles on the plasma membrane and the downstream delivery of internalized molecules to a number of cellular locations. As numerous Rabs are located to endocytic pathways, an internalized molecule may traverse a number of Rab specific substations or subdomains en route to its final destination. Rabs 5, 21 and 22 have all been localized to the early endocytic pathway and have been shown to share a number of characteristics to merit their segregation into a single functional endocytic group. In this review, we compare experiments that describe similarities and differences in endosome morphology and function that is mediated by their expression in cells.

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