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抑制铜绿假单胞菌的一种环氧化物水解酶毒力因子可保护囊性纤维化跨膜传导调节因子。

Inhibiting an Epoxide Hydrolase Virulence Factor from Pseudomonas aeruginosa Protects CFTR.

作者信息

Bahl Christopher D, Hvorecny Kelli L, Bomberger Jennifer M, Stanton Bruce A, Hammock Bruce D, Morisseau Christophe, Madden Dean R

机构信息

Department of Biochemistry, Geisel School of Medicine at Dartmouth, 7200 Vail Building, Hanover, NH 03755 (USA) http://www.dartmouth.edu/∼madden.

Department of Microbiology & Immunology, Geisel School of Medicine at Dartmouth, 7560 Vail Building, Hanover, NH 03755 (USA).

出版信息

Angew Chem Int Ed Engl. 2015 Aug 17;54(34):9881-5. doi: 10.1002/anie.201503983. Epub 2015 Jul 1.

Abstract

Opportunistic pathogens exploit diverse strategies to sabotage host defenses. Pseudomonas aeruginosa secretes the CFTR inhibitory factor Cif and thus triggers loss of CFTR, an ion channel required for airway mucociliary defense. However, the mechanism of action of Cif has remained unclear. It catalyzes epoxide hydrolysis, but there is no known role for natural epoxides in CFTR regulation. It was demonstrated that the hydrolase activity of Cif is strictly required for its effects on CFTR. A small-molecule inhibitor that protects this key component of the mucociliary defense system was also uncovered. These results provide a basis for targeting the distinctive virulence chemistry of Cif and suggest an unanticipated role of physiological epoxides in intracellular protein trafficking.

摘要

机会性致病菌利用多种策略来破坏宿主防御。铜绿假单胞菌分泌囊性纤维化跨膜传导调节因子(CFTR)抑制因子Cif,从而引发CFTR的丧失,CFTR是气道黏液纤毛防御所需的离子通道。然而,Cif的作用机制仍不清楚。它催化环氧化物水解,但天然环氧化物在CFTR调节中尚无已知作用。已证明Cif的水解酶活性对其影响CFTR的作用是严格必需的。还发现了一种保护黏液纤毛防御系统这一关键组成部分的小分子抑制剂。这些结果为针对Cif独特的毒力化学作用提供了基础,并提示了生理环氧化物在细胞内蛋白质运输中出人意料的作用。

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