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杀菌素——靶向细菌毒力的小分子

Pilicides-small molecules targeting bacterial virulence.

作者信息

Aberg Veronica, Almqvist Fredrik

机构信息

Department of Chemistry, Umeå University, SE-90187, Umeå, Sweden.

出版信息

Org Biomol Chem. 2007 Jun 21;5(12):1827-34. doi: 10.1039/b702397a. Epub 2007 Apr 20.

Abstract

In a time of emerging bacterial resistance there is a vital need for new targets and strategies in antibacterial therapy. Using uropathogenic Escherichia coli as a model pathogen we have developed a class of compounds, pilicides, which inhibit the formation of virulence-associated organelles termed pili. The pilicides interfere with a highly conserved bacterial assembly and secretion system called the chaperone-usher pathway, which is abundant in a vast number of Gram-negative pathogens and serves to assemble multi-protein surface fibers (pili/fimbriae). This class of compounds provides a platform to gain insight into important biological processes such as the molecular mechanisms of the chaperone-usher pathway and the sophisticated function of pili. Pili are primarily involved in bacterial adhesion, invasion and persistence to host defenses. On this basis, pilicides can aid the development of new antibacterial agents.

摘要

在细菌耐药性不断出现的时代,抗菌治疗迫切需要新的靶点和策略。我们以尿路致病性大肠杆菌作为模式病原体,开发了一类化合物——菌毛抑制剂,它能抑制称为菌毛的毒力相关细胞器的形成。菌毛抑制剂干扰一种高度保守的细菌组装和分泌系统,即伴侣-外膜蛋白途径,该途径在大量革兰氏阴性病原体中广泛存在,用于组装多蛋白表面纤维(菌毛/纤毛)。这类化合物提供了一个平台,有助于深入了解重要的生物学过程,如伴侣-外膜蛋白途径的分子机制和菌毛的复杂功能。菌毛主要参与细菌对宿主防御的黏附、侵袭和持续存在。在此基础上,菌毛抑制剂有助于新型抗菌药物的开发。

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