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细菌Sec转位酶处的交通堵塞:小分子抑制剂靶向SecA纳米马达

Traffic jam at the bacterial sec translocase: targeting the SecA nanomotor by small-molecule inhibitors.

作者信息

Segers Kenneth, Anné Jozef

机构信息

Laboratory of Bacteriology, Rega Institute for Medical Research, Katholieke Universiteit Leuven, 3000 Leuven, Belgium.

出版信息

Chem Biol. 2011 Jun 24;18(6):685-98. doi: 10.1016/j.chembiol.2011.04.007.

Abstract

The rapid rise of drug-resistant bacteria is one of the most serious unmet medical needs facing the world. Despite this increasing problem of antibiotic resistance, the number of different antibiotics available for the treatment of serious infections is dwindling. Therefore, there is an urgent need for new antibacterial drugs, preferably with novel modes of action to potentially avoid cross-resistance with existing antibacterial agents. In recent years, increasing attention has been paid to bacterial protein secretion as a potential antibacterial target. Among the different protein secretion pathways that are present in bacterial pathogens, the general protein secretory (Sec) pathway is widely considered as an attractive target for antibacterial therapy. One of the key components of the Sec pathway is the peripheral membrane ATPase SecA, which provides the energy for the translocation of preproteins across the bacterial cytoplasmic membrane. In this review, we will provide an overview of research efforts on the discovery and development of small-molecule SecA inhibitors. Furthermore, recent advances on the structure and function of SecA and their potential impact on antibacterial drug discovery will be discussed.

摘要

耐药细菌的迅速增加是全球面临的最严重的未满足医疗需求之一。尽管抗生素耐药性问题日益严重,但可用于治疗严重感染的不同抗生素数量却在减少。因此,迫切需要新型抗菌药物,最好具有新颖的作用模式,以避免与现有抗菌剂产生交叉耐药性。近年来,细菌蛋白分泌作为潜在的抗菌靶点受到了越来越多的关注。在细菌病原体中存在的不同蛋白分泌途径中,一般蛋白分泌(Sec)途径被广泛认为是抗菌治疗的一个有吸引力的靶点。Sec途径的关键成分之一是外周膜ATP酶SecA,它为前体蛋白跨细菌细胞质膜的转运提供能量。在这篇综述中,我们将概述小分子SecA抑制剂发现和开发的研究工作。此外,还将讨论SecA的结构和功能的最新进展及其对抗菌药物发现的潜在影响。

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