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

[Image: see text] 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...

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Autores principales: Al Nahas, Kareem, Fletcher, Marcus, Hammond, Katharine, Nehls, Christian, Cama, Jehangir, Ryadnov, Maxim G., Keyser, Ulrich F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9280716/
https://www.ncbi.nlm.nih.gov/pubmed/35760038
http://dx.doi.org/10.1021/acs.analchem.1c03564
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author Al Nahas, Kareem
Fletcher, Marcus
Hammond, Katharine
Nehls, Christian
Cama, Jehangir
Ryadnov, Maxim G.
Keyser, Ulrich F.
author_facet Al Nahas, Kareem
Fletcher, Marcus
Hammond, Katharine
Nehls, Christian
Cama, Jehangir
Ryadnov, Maxim G.
Keyser, Ulrich F.
author_sort Al Nahas, Kareem
collection PubMed
description [Image: see text] 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.
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spelling pubmed-92807162022-07-15 Measuring Thousands of Single-Vesicle Leakage Events Reveals the Mode of Action of Antimicrobial Peptides Al Nahas, Kareem Fletcher, Marcus Hammond, Katharine Nehls, Christian Cama, Jehangir Ryadnov, Maxim G. Keyser, Ulrich F. Anal Chem [Image: see text] 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. American Chemical Society 2022-06-27 2022-07-12 /pmc/articles/PMC9280716/ /pubmed/35760038 http://dx.doi.org/10.1021/acs.analchem.1c03564 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Al Nahas, Kareem
Fletcher, Marcus
Hammond, Katharine
Nehls, Christian
Cama, Jehangir
Ryadnov, Maxim G.
Keyser, Ulrich F.
Measuring Thousands of Single-Vesicle Leakage Events Reveals the Mode of Action of Antimicrobial Peptides
title Measuring Thousands of Single-Vesicle Leakage Events Reveals the Mode of Action of Antimicrobial Peptides
title_full Measuring Thousands of Single-Vesicle Leakage Events Reveals the Mode of Action of Antimicrobial Peptides
title_fullStr Measuring Thousands of Single-Vesicle Leakage Events Reveals the Mode of Action of Antimicrobial Peptides
title_full_unstemmed Measuring Thousands of Single-Vesicle Leakage Events Reveals the Mode of Action of Antimicrobial Peptides
title_short Measuring Thousands of Single-Vesicle Leakage Events Reveals the Mode of Action of Antimicrobial Peptides
title_sort measuring thousands of single-vesicle leakage events reveals the mode of action of antimicrobial peptides
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9280716/
https://www.ncbi.nlm.nih.gov/pubmed/35760038
http://dx.doi.org/10.1021/acs.analchem.1c03564
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