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Measuring Thousands of Single-Vesicle Leakage Events Reveals the Mode of Action of Antimicrobial Peptides

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ANALYTICAL CHEMISTRY
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AMER CHEMICAL SOC
DOI: 10.1021/acs.analchem.1c03564

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This study used a highly parallelized microfluidic platform to conduct quantitative long-term microscopy studies on the membrane-disruptive activity of antimicrobial peptides, revealing the relationship between the modes of action and the molecular activity mechanisms of these peptides.
ABSTRACT: Host defense or antimicrobial peptides hold promise for providing new pipelines of effective antimicrobial 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.

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