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一种弧菌效应蛋白是一种肌醇磷酸酶,破坏宿主细胞膜的完整性。

A Vibrio effector protein is an inositol phosphatase and disrupts host cell membrane integrity.

机构信息

Department of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.

出版信息

Science. 2010 Sep 24;329(5999):1660-2. doi: 10.1126/science.1192850. Epub 2010 Aug 19.

Abstract

The marine bacterium Vibrio parahaemolyticus causes gastroenteritis in humans and encodes the type III effector protein VPA0450, which contributes to host cell death caused by autophagy, cell rounding, and cell lysis. We found that VPA0450 is an inositol polyphosphate 5-phosphatase that hydrolyzed the D5 phosphate from the plasma membrane phospholipid phosphatidylinositol 4,5-bisphosphate. VPA0450 disrupted cytoskeletal binding sites on the inner surface of membranes of human cells and caused plasma membrane blebbing, which compromised membrane integrity and probably contributed to cell death by facilitating lysis. Thus, bacterial pathogens can disrupt adaptor protein-binding sites required for proper membrane and cytoskeleton dynamics by altering the homeostasis of membrane-bound inositol-signaling molecules.

摘要

海洋细菌副溶血性弧菌可引起人类肠胃炎,并编码 III 型效应蛋白 VPA0450,该蛋白有助于自噬、细胞圆化和细胞裂解引起的宿主细胞死亡。我们发现 VPA0450 是一种肌醇多磷酸 5-磷酸酶,可从质膜磷脂磷脂酰肌醇 4,5-二磷酸中水解 D5 磷酸。VPA0450 破坏了人细胞内膜内表面的细胞骨架结合位点,并导致质膜起泡,这破坏了膜的完整性,并可能通过促进裂解而导致细胞死亡。因此,细菌病原体可以通过改变膜结合的肌醇信号分子的内稳态来破坏适当的膜和细胞骨架动态所需的衔接蛋白结合位点。

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