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In-cell DNP NMR reveals multiple targeting effect of antimicrobial peptide

Dynamic nuclear polarization NMR spectroscopy was used to investigate the effect of the antimicrobial peptide (AMP) maculatin 1.1 on E. coli cells. The enhanced (15)N NMR signals from nucleic acids, proteins and lipids identified a number of unanticipated physiological responses to peptide stress, r...

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Autores principales: Separovic, Frances, Hofferek, Vinzenz, Duff, Anthony P., McConville, Malcom J., Sani, Marc-Antoine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9486116/
https://www.ncbi.nlm.nih.gov/pubmed/36147732
http://dx.doi.org/10.1016/j.yjsbx.2022.100074
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author Separovic, Frances
Hofferek, Vinzenz
Duff, Anthony P.
McConville, Malcom J.
Sani, Marc-Antoine
author_facet Separovic, Frances
Hofferek, Vinzenz
Duff, Anthony P.
McConville, Malcom J.
Sani, Marc-Antoine
author_sort Separovic, Frances
collection PubMed
description Dynamic nuclear polarization NMR spectroscopy was used to investigate the effect of the antimicrobial peptide (AMP) maculatin 1.1 on E. coli cells. The enhanced (15)N NMR signals from nucleic acids, proteins and lipids identified a number of unanticipated physiological responses to peptide stress, revealing that membrane-active AMPs can have a multi-target impact on E. coli cells. DNP-enhanced (15)N-observed (31)P-dephased REDOR NMR allowed monitoring how Mac1 induced DNA condensation and prevented intermolecular salt bridges between the main E. coli lipid phosphatidylethanolamine (PE) molecules. The latter was supported by similar results obtained using E. coli PE lipid systems. Overall, the ability to monitor the action of antimicrobial peptides in situ will provide greater insight into their mode of action.
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spelling pubmed-94861162022-09-21 In-cell DNP NMR reveals multiple targeting effect of antimicrobial peptide Separovic, Frances Hofferek, Vinzenz Duff, Anthony P. McConville, Malcom J. Sani, Marc-Antoine J Struct Biol X Advances in biomolecular structure and dynamics elucidation by solid-state NMR Dynamic nuclear polarization NMR spectroscopy was used to investigate the effect of the antimicrobial peptide (AMP) maculatin 1.1 on E. coli cells. The enhanced (15)N NMR signals from nucleic acids, proteins and lipids identified a number of unanticipated physiological responses to peptide stress, revealing that membrane-active AMPs can have a multi-target impact on E. coli cells. DNP-enhanced (15)N-observed (31)P-dephased REDOR NMR allowed monitoring how Mac1 induced DNA condensation and prevented intermolecular salt bridges between the main E. coli lipid phosphatidylethanolamine (PE) molecules. The latter was supported by similar results obtained using E. coli PE lipid systems. Overall, the ability to monitor the action of antimicrobial peptides in situ will provide greater insight into their mode of action. Elsevier 2022-09-13 /pmc/articles/PMC9486116/ /pubmed/36147732 http://dx.doi.org/10.1016/j.yjsbx.2022.100074 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Advances in biomolecular structure and dynamics elucidation by solid-state NMR
Separovic, Frances
Hofferek, Vinzenz
Duff, Anthony P.
McConville, Malcom J.
Sani, Marc-Antoine
In-cell DNP NMR reveals multiple targeting effect of antimicrobial peptide
title In-cell DNP NMR reveals multiple targeting effect of antimicrobial peptide
title_full In-cell DNP NMR reveals multiple targeting effect of antimicrobial peptide
title_fullStr In-cell DNP NMR reveals multiple targeting effect of antimicrobial peptide
title_full_unstemmed In-cell DNP NMR reveals multiple targeting effect of antimicrobial peptide
title_short In-cell DNP NMR reveals multiple targeting effect of antimicrobial peptide
title_sort in-cell dnp nmr reveals multiple targeting effect of antimicrobial peptide
topic Advances in biomolecular structure and dynamics elucidation by solid-state NMR
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9486116/
https://www.ncbi.nlm.nih.gov/pubmed/36147732
http://dx.doi.org/10.1016/j.yjsbx.2022.100074
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