在他们的盔甲上制造缺口:针对细菌细胞包膜的当前和下一代抗菌策略。

2区 生物学 Q1 Biochemistry, Genetics and Molecular Biology Advances in Microbial Physiology Pub Date : 2023-01-01 Epub Date: 2023-06-27 DOI:10.1016/bs.ampbs.2023.05.003
Nikol Kadeřábková, Ayesha J S Mahmood, R Christopher D Furniss, Despoina A I Mavridou
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引用次数: 0

摘要

革兰氏阴性菌具有独特的战胜抗生素的能力。它们的最外层,细胞包膜,是一个天然的渗透屏障,包含一系列能够中和大多数现有抗菌药物的抗性蛋白。因此,它的存在为耐药性感染的治疗和新抗生素的开发制造了主要障碍。尽管有这种看似难以穿透的盔甲,但对细胞包膜的深入了解,包括结构、功能和系统生物学的见解,推动了针对它的努力,最终可以产生新的抗菌疗法。在这篇文章中,我们大致概述了细胞包膜的生物学,并强调了在产生损害其功能或生物发生的抑制剂方面的尝试和成功。我们认为,几十年来阻碍抗生素发现的结构,在设计针对细菌病原体的新一代治疗方法方面具有尚未开发的潜力。
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Making a chink in their armor: Current and next-generation antimicrobial strategies against the bacterial cell envelope.

Gram-negative bacteria are uniquely equipped to defeat antibiotics. Their outermost layer, the cell envelope, is a natural permeability barrier that contains an array of resistance proteins capable of neutralizing most existing antimicrobials. As a result, its presence creates a major obstacle for the treatment of resistant infections and for the development of new antibiotics. Despite this seemingly impenetrable armor, in-depth understanding of the cell envelope, including structural, functional and systems biology insights, has promoted efforts to target it that can ultimately lead to the generation of new antibacterial therapies. In this article, we broadly overview the biology of the cell envelope and highlight attempts and successes in generating inhibitors that impair its function or biogenesis. We argue that the very structure that has hampered antibiotic discovery for decades has untapped potential for the design of novel next-generation therapeutics against bacterial pathogens.

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来源期刊
Advances in Microbial Physiology
Advances in Microbial Physiology 生物-生化与分子生物学
CiteScore
6.20
自引率
0.00%
发文量
16
期刊介绍: Advances in Microbial Physiology publishes topical and important reviews, interpreting physiology to include all material that contributes to our understanding of how microorganisms and their component parts work. First published in 1967, the editors have always striven to interpret microbial physiology in the broadest context and have never restricted the contents to traditional views of whole cell physiology.
期刊最新文献
Preface. Biological functions of bacterial lysophospholipids. Redefining the bacterial Type I protein secretion system. Purine catabolism by enterobacteria. Fumarate, a central electron acceptor for Enterobacteriaceae beyond fumarate respiration and energy conservation.
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