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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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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. |
format | Online Article Text |
id | pubmed-9486116 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
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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