吸收并释放:细菌可以随意使用Rab1小GTPase。

Yunhao Tan, Zhao-Qing Luo
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引用次数: 4

摘要

成功的病原体能够利用宿主细胞的信号通路,建立有利于其生存和增殖的生态位。一个新出现的例子是胞内病原体嗜肺军团菌的毒力因子对小GTPase Rab1的调节。除了模拟宿主调控因子参与控制Rab1活性的蛋白质外,这种细菌还通过AMPylation将这种小的GTPase暂时锁定在其活性形式。细菌吞噬体中Rab1的有效释放需要在被细菌GAP蛋白LepB灭活之前进行去氨酰基化。在自然条件下,Rab活性是否受到类似的调节尚不清楚,但很明显,来自病原体的毒力因子可以成为解剖宿主细胞过程复杂性的宝贵工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Take it and release it: The use of the Rab1 small GTPase at a bacterium's will.

Successful pathogens are equipped to exploit the signaling pathways of their host cell to establish a niche conducive for their survival and proliferation. One emerging example is the modulation of the small GTPase Rab1 by virulence factors of the intracellular pathogen Legionella pneumophila. Besides proteins that mimic host regulatory factors involved in controlling Rab1 activity, this bacterium temporally locks this small GTPase in its active form by AMPylation. Efficient release of Rab1 from the bacterial phagosome requires deAMPylation prior to being inactivated by the bacterial GAP protein LepB. Whether Rab activity is similarly regulated under native condition is unknown, but it is clear that virulence factors from pathogens can be invaluable tools in dissecting the intricacy of host cellular processes.

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