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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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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. |
format | Online Article Text |
id | pubmed-9280716 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
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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