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抑制革兰氏阴性菌外膜组装机器的抗菌剂。

Antimicrobial Agents That Inhibit the Outer Membrane Assembly Machines of Gram-Negative Bacteria.

作者信息

Choi Umji, Lee Chang-Ro

机构信息

Department of Bioscience and Bioinformatics, Myongji University, Yongin 17058, Republic of Korea.

出版信息

J Microbiol Biotechnol. 2019 Jan 28;29(1):1-10. doi: 10.4014/jmb.1804.03051.

Abstract

Gram-negative pathogens, such as , , and , pose a serious threat to public health worldwide, due to high rates of antibiotic resistance and the lack of development of novel antimicrobial agents targeting Gram-negative bacteria. The outer membrane (OM) of Gram-negative bacteria is a unique architecture that acts as a potent permeability barrier against toxic molecules, such as antibiotics. The OM is composed of phospholipids, lipopolysaccharide (LPS), outer membrane β-barrel proteins (OMP), and lipoproteins. These components are synthesized in the cytoplasm or in the inner membrane, and are then selectively transported to the OM by the specific transport machines, including the Lol, BAM, and Lpt pathways. In this review, we summarize recent studies on the assembly systems of OM components and analyze studies for the development of inhibitors that target these systems. These analyses show that OM assembly machines have the potential to be a novel attractive drug target of Gram-negative bacteria.

摘要

革兰氏阴性病原体,如大肠杆菌、肺炎克雷伯菌和鲍曼不动杆菌,由于抗生素耐药率高以及缺乏针对革兰氏阴性菌的新型抗菌药物,对全球公共卫生构成严重威胁。革兰氏阴性菌的外膜(OM)是一种独特的结构,可作为对抗有毒分子(如抗生素)的有效渗透屏障。外膜由磷脂、脂多糖(LPS)、外膜β-桶蛋白(OMP)和脂蛋白组成。这些成分在细胞质或内膜中合成,然后通过特定的转运机制,包括Lol、BAM和Lpt途径,选择性地转运到外膜。在本综述中,我们总结了外膜成分组装系统的最新研究,并分析了针对这些系统的抑制剂开发研究。这些分析表明,外膜组装机制有可能成为革兰氏阴性菌一种新的有吸引力的药物靶点。

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