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铜绿假单胞菌外毒素S和外毒素T。

Pseudomonas aeruginosa ExoS and ExoT.

作者信息

Barbieri J T, Sun J

机构信息

Microbiology and Molecular Genetics, Medical College of Wisconsin, 8701 Watertown Plk. Road, Milwaukee, WI 53226, USA.

出版信息

Rev Physiol Biochem Pharmacol. 2004;152:79-92. doi: 10.1007/s10254-004-0031-7. Epub 2004 Aug 24.

Abstract

ExoS and ExoT are bi-functional type-III cytotoxins of Pseudomonas aeruginosa that share 76% primary amino acid homology and contain N-terminal RhoGAP domains and C-terminal ADP-ribosylation domains. The Rho GAP activities of ExoS and ExoT appear to be biochemically and biologically identical, targeting Rho, Rac, and Cdc42. Expression of the RhoGAP domain in mammalian cells results in the disruption of the actin cytoskeleton and interference of phagocytosis. Expression of the ADP-ribosyltransferase domain of ExoS elicits a cytotoxic phenotype in cultured cells, while expression of ExoT appears to interfere with host cell phagocytic activity. Recent studies showed that ExoS and ExoT ADP-ribosylate different substrates. While ExoS has poly-substrate specificity and can ADP-ribosylate numerous host proteins, ExoT ADP-ribosylates a more restricted subset of host proteins including the Crk proteins. Protein modeling predicts that electrostatic interactions contribute to the substrate specificity of the ADP-ribosyltransferase domains of ExoS and ExoT.

摘要

外毒素S(ExoS)和外毒素T(ExoT)是铜绿假单胞菌的双功能III型细胞毒素,它们的一级氨基酸同源性为76%,包含N端的RhoGAP结构域和C端的ADP核糖基化结构域。ExoS和ExoT的RhoGAP活性在生化和生物学上似乎是相同的,作用于Rho、Rac和Cdc42。RhoGAP结构域在哺乳动物细胞中的表达会导致肌动蛋白细胞骨架的破坏和吞噬作用的干扰。ExoS的ADP核糖基转移酶结构域的表达在培养细胞中引发细胞毒性表型,而ExoT的表达似乎会干扰宿主细胞的吞噬活性。最近的研究表明,ExoS和ExoT会对不同的底物进行ADP核糖基化。ExoS具有多底物特异性,可对多种宿主蛋白进行ADP核糖基化,而ExoT仅对包括Crk蛋白在内的更有限的宿主蛋白子集进行ADP核糖基化。蛋白质建模预测,静电相互作用有助于ExoS和ExoT的ADP核糖基转移酶结构域的底物特异性。

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