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多少抗菌肽分子能杀死一个细菌?以PMAP - 23为例。

How many antimicrobial peptide molecules kill a bacterium? The case of PMAP-23.

作者信息

Roversi Daniela, Luca Vincenzo, Aureli Simone, Park Yoonkyung, Mangoni Maria Luisa, Stella Lorenzo

机构信息

Department of Chemical Sciences and Technologies, University of Rome Tor Vergata , 00133 Rome, Italy.

出版信息

ACS Chem Biol. 2014 Sep 19;9(9):2003-7. doi: 10.1021/cb500426r. Epub 2014 Jul 30.

Abstract

Antimicrobial peptides (AMPs) kill bacteria mainly through the perturbation of their membranes and are promising compounds to fight drug resistance. Models of the mechanism of AMPs-induced membrane perturbation were developed based on experiments in liposomes, but their relevance for bacterial killing is debated. We determined the association of an analogue of the AMP PMAP-23 to Escherichia coli cells, under the same experimental conditions used to measure bactericidal activity. Killing took place only when bound peptides completely saturated bacterial membranes (10(6)-10(7) bound peptides per cell), indicating that the "carpet" model for the perturbation of artificial bilayers is representative of what happens in real bacteria. This finding supports the view that, at least for this peptide, a microbicidal mechanism is possible in vivo only at micromolar total peptide concentrations. We also showed that, notwithstanding their simplicity, liposomes represent a reliable model to characterize AMPs partition in bacterial membranes.

摘要

抗菌肽(AMPs)主要通过扰乱细菌细胞膜来杀死细菌,是对抗耐药性的有前景的化合物。基于脂质体实验建立了AMPs诱导膜扰动机制的模型,但它们与细菌杀伤的相关性存在争议。在用于测量杀菌活性的相同实验条件下,我们确定了AMPs类似物PMAP - 23与大肠杆菌细胞的结合情况。只有当结合的肽完全饱和细菌细胞膜时(每个细胞有10⁶ - 10⁷个结合的肽)才会发生杀伤作用,这表明人工双层膜扰动的“地毯”模型代表了真实细菌中的情况。这一发现支持了这样一种观点,即至少对于这种肽来说,只有在微摩尔级的总肽浓度下,体内才可能存在杀菌机制。我们还表明,尽管脂质体很简单,但它们是表征AMPs在细菌膜中分配的可靠模型。

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