Cavendish Laboratory, University of Cambridge, J.J. Thomson Avenue, Cambridge CB3 0HE, U.K.
National Physical Laboratory, Hampton Road, Teddington TW11 0LW, U.K.
Anal Chem. 2022 Jul 12;94(27):9530-9539. doi: 10.1021/acs.analchem.1c03564. Epub 2022 Jun 27.
Host defense or antimicrobial peptides hold promise for providing new pipelines of effective antimicrobial agents. Their activity quantified against model phospholipid membranes is fundamental to a detailed understanding of their structure-activity relationships. However, classical characterization assays often lack the ability to achieve this insight. Leveraging a highly parallelized microfluidic platform for trapping and studying thousands of giant unilamellar vesicles, we conducted quantitative long-term microscopy studies to monitor the membrane-disruptive activity of archetypal antimicrobial peptides with a high spatiotemporal resolution. We described the modes of action of these peptides via measurements of the disruption of the vesicle population under the conditions of continuous peptide dosing using a range of concentrations and related the observed modes to the molecular activity mechanisms of these peptides. The study offers an effective approach for characterizing membrane-targeting antimicrobial agents in a standardized manner and for assigning specific modes of action to the corresponding antimicrobial mechanisms.
宿主防御或抗菌肽有望提供新的有效抗菌药物。对模型磷脂膜的活性定量是深入了解其结构-活性关系的基础。然而,经典的表征方法往往缺乏实现这一目标的能力。利用高度并行的微流控平台来捕获和研究数千个巨大的单层囊泡,我们进行了定量的长期显微镜研究,以高时空分辨率监测典型抗菌肽的膜破坏活性。我们通过测量在连续肽给药条件下,使用一系列浓度,对囊泡群体的破坏情况,描述了这些肽的作用模式,并将观察到的模式与这些肽的分子作用机制相关联。该研究提供了一种有效的方法,用于以标准化的方式表征靶向膜的抗菌剂,并将特定的作用模式分配给相应的抗菌机制。