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军团菌效应蛋白 RavZ 通过不可逆的 Atg8 去共轭作用抑制宿主自噬。

The Legionella effector RavZ inhibits host autophagy through irreversible Atg8 deconjugation.

机构信息

Department of Microbial Pathogenesis, Yale University School of Medicine, New Haven, CT, USA.

出版信息

Science. 2012 Nov 23;338(6110):1072-6. doi: 10.1126/science.1227026. Epub 2012 Oct 25.

Abstract

Eukaryotic cells can use the autophagy pathway to defend against microbes that gain access to the cytosol or reside in pathogen-modified vacuoles. It remains unclear if pathogens have evolved specific mechanisms to manipulate autophagy. Here, we found that the intracellular pathogen Legionella pneumophila could interfere with autophagy by using the bacterial effector protein RavZ to directly uncouple Atg8 proteins attached to phosphatidylethanolamine on autophagosome membranes. RavZ hydrolyzed the amide bond between the carboxyl-terminal glycine residue and an adjacent aromatic residue in Atg8 proteins, producing an Atg8 protein that could not be reconjugated by Atg7 and Atg3. Thus, intracellular pathogens can inhibit autophagy by irreversibly inactivating Atg8 proteins during infection.

摘要

真核细胞可以利用自噬途径来抵御进入细胞质或存在于被病原体修饰的空泡中的微生物。目前尚不清楚病原体是否进化出特定的机制来操纵自噬。在这里,我们发现,胞内病原体军团菌可以通过使用细菌效应蛋白 RavZ 直接解偶联附着在自噬体膜上的磷脂酰乙醇胺的 Atg8 蛋白,来干扰自噬。RavZ 水解 Atg8 蛋白羧基末端甘氨酸残基和相邻芳香族残基之间的酰胺键,产生一种不能被 Atg7 和 Atg3 重新共轭的 Atg8 蛋白。因此,胞内病原体可以通过在感染过程中不可逆地使 Atg8 蛋白失活来抑制自噬。

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