Marcellini Ludovica, Giammatteo Maria, Aimola Pierpaolo, Mangoni Maria Luisa
Istituto Pasteur-Fondazione Cenci Bolognetti, Dipartimento di Scienze Biochimiche, Università La Sapienza, Roma, Italy.
Methods Mol Biol. 2010;618:249-66. doi: 10.1007/978-1-60761-594-1_16.
Due to the increasing resistance of microbial pathogens to the available drugs, the identification of new antimicrobial agents with a new mechanism of action is urgently needed. In this context, cationic antimicrobial peptides (AMPs) are considered promising candidates. Although there is evidence that, in contrast to conventional antibiotics, microbial membranes are the principal target of a large number of AMPs, thus making it difficult for the pathogen to acquire resistance, their mode(s) of action is not yet completely clear. Intense research is currently devoted to understand the effect(s) of AMPs on intact cells, either at sub-lethal or at lethal peptide concentrations, and fluorescence/electron microscopy techniques represent a valid tool to get insight into the damage caused by these molecules on the morphology and membrane structure of the target cell. We here present an overview of some microscopic methodologies to address this issue.
由于微生物病原体对现有药物的耐药性不断增加,迫切需要鉴定具有新作用机制的新型抗菌剂。在这种背景下,阳离子抗菌肽(AMPs)被认为是有前途的候选者。尽管有证据表明,与传统抗生素不同,微生物膜是大量AMPs的主要靶标,因此病原体难以获得耐药性,但其作用方式尚未完全明确。目前正在进行深入研究,以了解AMPs在亚致死或致死肽浓度下对完整细胞的影响,而荧光/电子显微镜技术是深入了解这些分子对靶细胞形态和膜结构造成损伤的有效工具。我们在此概述一些用于解决此问题的微观方法。