Cargando…
Insight into the Mechanism of Action and Peptide‐Membrane Interactions of Aib‐Rich Peptides: Multitechnique Experimental and Theoretical Analysis
The increase in resistant bacterial strains necessitates the identification of new antimicrobial molecules. Antimicrobial peptides (AMPs) are an attractive option because of evidence that bacteria cannot easily develop resistance to AMPs. The peptaibols, a class of naturally occurring AMPs, have sho...
Autores principales: | , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8248331/ https://www.ncbi.nlm.nih.gov/pubmed/33411956 http://dx.doi.org/10.1002/cbic.202000834 |
_version_ | 1783716699898380288 |
---|---|
author | Lizio, Maria Giovanna Campana, Mario De Poli, Matteo Jefferies, Damien F. Cullen, William Andrushchenko, Valery Chmel, Nikola P. Bouř, Petr Khalid, Syma Clayden, Jonathan Blanch, Ewan Rodger, Alison Webb, Simon J. |
author_facet | Lizio, Maria Giovanna Campana, Mario De Poli, Matteo Jefferies, Damien F. Cullen, William Andrushchenko, Valery Chmel, Nikola P. Bouř, Petr Khalid, Syma Clayden, Jonathan Blanch, Ewan Rodger, Alison Webb, Simon J. |
author_sort | Lizio, Maria Giovanna |
collection | PubMed |
description | The increase in resistant bacterial strains necessitates the identification of new antimicrobial molecules. Antimicrobial peptides (AMPs) are an attractive option because of evidence that bacteria cannot easily develop resistance to AMPs. The peptaibols, a class of naturally occurring AMPs, have shown particular promise as antimicrobial drugs, but their development has been hindered by their mechanism of action not being clearly understood. To explore how peptaibols might interact with membranes, circular dichroism, vibrational circular dichroism, linear dichroism, Raman spectroscopy, Raman optical activity, neutron reflectivity and molecular dynamics simulations have been used to study a small library of peptaibol mimics, the Aib‐rich peptides. All the peptides studied quickly partitioned and oriented in membranes, and we found evidence of chiral interactions between the phospholipids and membrane‐embedded peptides. The protocols presented in this paper open new ground by showing how chiro‐optical spectroscopies can throw light on the mechanism of action of AMPs. |
format | Online Article Text |
id | pubmed-8248331 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-82483312021-07-06 Insight into the Mechanism of Action and Peptide‐Membrane Interactions of Aib‐Rich Peptides: Multitechnique Experimental and Theoretical Analysis Lizio, Maria Giovanna Campana, Mario De Poli, Matteo Jefferies, Damien F. Cullen, William Andrushchenko, Valery Chmel, Nikola P. Bouř, Petr Khalid, Syma Clayden, Jonathan Blanch, Ewan Rodger, Alison Webb, Simon J. Chembiochem Full Papers The increase in resistant bacterial strains necessitates the identification of new antimicrobial molecules. Antimicrobial peptides (AMPs) are an attractive option because of evidence that bacteria cannot easily develop resistance to AMPs. The peptaibols, a class of naturally occurring AMPs, have shown particular promise as antimicrobial drugs, but their development has been hindered by their mechanism of action not being clearly understood. To explore how peptaibols might interact with membranes, circular dichroism, vibrational circular dichroism, linear dichroism, Raman spectroscopy, Raman optical activity, neutron reflectivity and molecular dynamics simulations have been used to study a small library of peptaibol mimics, the Aib‐rich peptides. All the peptides studied quickly partitioned and oriented in membranes, and we found evidence of chiral interactions between the phospholipids and membrane‐embedded peptides. The protocols presented in this paper open new ground by showing how chiro‐optical spectroscopies can throw light on the mechanism of action of AMPs. John Wiley and Sons Inc. 2021-02-24 2021-05-04 /pmc/articles/PMC8248331/ /pubmed/33411956 http://dx.doi.org/10.1002/cbic.202000834 Text en © 2021 The Authors. ChemBioChem published by Wiley-VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Full Papers Lizio, Maria Giovanna Campana, Mario De Poli, Matteo Jefferies, Damien F. Cullen, William Andrushchenko, Valery Chmel, Nikola P. Bouř, Petr Khalid, Syma Clayden, Jonathan Blanch, Ewan Rodger, Alison Webb, Simon J. Insight into the Mechanism of Action and Peptide‐Membrane Interactions of Aib‐Rich Peptides: Multitechnique Experimental and Theoretical Analysis |
title | Insight into the Mechanism of Action and Peptide‐Membrane Interactions of Aib‐Rich Peptides: Multitechnique Experimental and Theoretical Analysis |
title_full | Insight into the Mechanism of Action and Peptide‐Membrane Interactions of Aib‐Rich Peptides: Multitechnique Experimental and Theoretical Analysis |
title_fullStr | Insight into the Mechanism of Action and Peptide‐Membrane Interactions of Aib‐Rich Peptides: Multitechnique Experimental and Theoretical Analysis |
title_full_unstemmed | Insight into the Mechanism of Action and Peptide‐Membrane Interactions of Aib‐Rich Peptides: Multitechnique Experimental and Theoretical Analysis |
title_short | Insight into the Mechanism of Action and Peptide‐Membrane Interactions of Aib‐Rich Peptides: Multitechnique Experimental and Theoretical Analysis |
title_sort | insight into the mechanism of action and peptide‐membrane interactions of aib‐rich peptides: multitechnique experimental and theoretical analysis |
topic | Full Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8248331/ https://www.ncbi.nlm.nih.gov/pubmed/33411956 http://dx.doi.org/10.1002/cbic.202000834 |
work_keys_str_mv | AT liziomariagiovanna insightintothemechanismofactionandpeptidemembraneinteractionsofaibrichpeptidesmultitechniqueexperimentalandtheoreticalanalysis AT campanamario insightintothemechanismofactionandpeptidemembraneinteractionsofaibrichpeptidesmultitechniqueexperimentalandtheoreticalanalysis AT depolimatteo insightintothemechanismofactionandpeptidemembraneinteractionsofaibrichpeptidesmultitechniqueexperimentalandtheoreticalanalysis AT jefferiesdamienf insightintothemechanismofactionandpeptidemembraneinteractionsofaibrichpeptidesmultitechniqueexperimentalandtheoreticalanalysis AT cullenwilliam insightintothemechanismofactionandpeptidemembraneinteractionsofaibrichpeptidesmultitechniqueexperimentalandtheoreticalanalysis AT andrushchenkovalery insightintothemechanismofactionandpeptidemembraneinteractionsofaibrichpeptidesmultitechniqueexperimentalandtheoreticalanalysis AT chmelnikolap insightintothemechanismofactionandpeptidemembraneinteractionsofaibrichpeptidesmultitechniqueexperimentalandtheoreticalanalysis AT bourpetr insightintothemechanismofactionandpeptidemembraneinteractionsofaibrichpeptidesmultitechniqueexperimentalandtheoreticalanalysis AT khalidsyma insightintothemechanismofactionandpeptidemembraneinteractionsofaibrichpeptidesmultitechniqueexperimentalandtheoreticalanalysis AT claydenjonathan insightintothemechanismofactionandpeptidemembraneinteractionsofaibrichpeptidesmultitechniqueexperimentalandtheoreticalanalysis AT blanchewan insightintothemechanismofactionandpeptidemembraneinteractionsofaibrichpeptidesmultitechniqueexperimentalandtheoreticalanalysis AT rodgeralison insightintothemechanismofactionandpeptidemembraneinteractionsofaibrichpeptidesmultitechniqueexperimentalandtheoreticalanalysis AT webbsimonj insightintothemechanismofactionandpeptidemembraneinteractionsofaibrichpeptidesmultitechniqueexperimentalandtheoreticalanalysis |