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Engineering monolayer poration for rapid exfoliation of microbial membranes

The spread of bacterial resistance to traditional antibiotics continues to stimulate the search for alternative antimicrobial strategies. All forms of life, from bacteria to humans, are postulated to rely on a fundamental host defense mechanism, which exploits the formation of open pores in microbia...

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Autores principales: Pyne, Alice, Pfeil, Marc-Philipp, Bennett, Isabel, Ravi, Jascindra, Iavicoli, Patrizia, Lamarre, Baptiste, Roethke, Anita, Ray, Santanu, Jiang, Haibo, Bella, Angelo, Reisinger, Bernd, Yin, Daniel, Little, Benjamin, Muñoz-García, Juan C., Cerasoli, Eleonora, Judge, Peter J., Faruqui, Nilofar, Calzolai, Luigi, Henrion, Andre, Martyna, Glenn J., Grovenor, Chris R. M., Crain, Jason, Hoogenboom, Bart W., Watts, Anthony, Ryadnov, Maxim G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5369539/
https://www.ncbi.nlm.nih.gov/pubmed/28451250
http://dx.doi.org/10.1039/c6sc02925f
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author Pyne, Alice
Pfeil, Marc-Philipp
Bennett, Isabel
Ravi, Jascindra
Iavicoli, Patrizia
Lamarre, Baptiste
Roethke, Anita
Ray, Santanu
Jiang, Haibo
Bella, Angelo
Reisinger, Bernd
Yin, Daniel
Little, Benjamin
Muñoz-García, Juan C.
Cerasoli, Eleonora
Judge, Peter J.
Faruqui, Nilofar
Calzolai, Luigi
Henrion, Andre
Martyna, Glenn J.
Grovenor, Chris R. M.
Crain, Jason
Hoogenboom, Bart W.
Watts, Anthony
Ryadnov, Maxim G.
author_facet Pyne, Alice
Pfeil, Marc-Philipp
Bennett, Isabel
Ravi, Jascindra
Iavicoli, Patrizia
Lamarre, Baptiste
Roethke, Anita
Ray, Santanu
Jiang, Haibo
Bella, Angelo
Reisinger, Bernd
Yin, Daniel
Little, Benjamin
Muñoz-García, Juan C.
Cerasoli, Eleonora
Judge, Peter J.
Faruqui, Nilofar
Calzolai, Luigi
Henrion, Andre
Martyna, Glenn J.
Grovenor, Chris R. M.
Crain, Jason
Hoogenboom, Bart W.
Watts, Anthony
Ryadnov, Maxim G.
author_sort Pyne, Alice
collection PubMed
description The spread of bacterial resistance to traditional antibiotics continues to stimulate the search for alternative antimicrobial strategies. All forms of life, from bacteria to humans, are postulated to rely on a fundamental host defense mechanism, which exploits the formation of open pores in microbial phospholipid bilayers. Here we predict that transmembrane poration is not necessary for antimicrobial activity and reveal a distinct poration mechanism that targets the outer leaflet of phospholipid bilayers. Using a combination of molecular-scale and real-time imaging, spectroscopy and spectrometry approaches, we introduce a structural motif with a universal insertion mode in reconstituted membranes and live bacteria. We demonstrate that this motif rapidly assembles into monolayer pits that coalesce during progressive membrane exfoliation, leading to bacterial cell death within minutes. The findings offer a new physical basis for designing effective antibiotics.
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spelling pubmed-53695392017-04-27 Engineering monolayer poration for rapid exfoliation of microbial membranes Pyne, Alice Pfeil, Marc-Philipp Bennett, Isabel Ravi, Jascindra Iavicoli, Patrizia Lamarre, Baptiste Roethke, Anita Ray, Santanu Jiang, Haibo Bella, Angelo Reisinger, Bernd Yin, Daniel Little, Benjamin Muñoz-García, Juan C. Cerasoli, Eleonora Judge, Peter J. Faruqui, Nilofar Calzolai, Luigi Henrion, Andre Martyna, Glenn J. Grovenor, Chris R. M. Crain, Jason Hoogenboom, Bart W. Watts, Anthony Ryadnov, Maxim G. Chem Sci Chemistry The spread of bacterial resistance to traditional antibiotics continues to stimulate the search for alternative antimicrobial strategies. All forms of life, from bacteria to humans, are postulated to rely on a fundamental host defense mechanism, which exploits the formation of open pores in microbial phospholipid bilayers. Here we predict that transmembrane poration is not necessary for antimicrobial activity and reveal a distinct poration mechanism that targets the outer leaflet of phospholipid bilayers. Using a combination of molecular-scale and real-time imaging, spectroscopy and spectrometry approaches, we introduce a structural motif with a universal insertion mode in reconstituted membranes and live bacteria. We demonstrate that this motif rapidly assembles into monolayer pits that coalesce during progressive membrane exfoliation, leading to bacterial cell death within minutes. The findings offer a new physical basis for designing effective antibiotics. Royal Society of Chemistry 2017-02-01 2016-09-26 /pmc/articles/PMC5369539/ /pubmed/28451250 http://dx.doi.org/10.1039/c6sc02925f Text en This journal is © The Royal Society of Chemistry 2016 http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial 3.0 Unported License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Chemistry
Pyne, Alice
Pfeil, Marc-Philipp
Bennett, Isabel
Ravi, Jascindra
Iavicoli, Patrizia
Lamarre, Baptiste
Roethke, Anita
Ray, Santanu
Jiang, Haibo
Bella, Angelo
Reisinger, Bernd
Yin, Daniel
Little, Benjamin
Muñoz-García, Juan C.
Cerasoli, Eleonora
Judge, Peter J.
Faruqui, Nilofar
Calzolai, Luigi
Henrion, Andre
Martyna, Glenn J.
Grovenor, Chris R. M.
Crain, Jason
Hoogenboom, Bart W.
Watts, Anthony
Ryadnov, Maxim G.
Engineering monolayer poration for rapid exfoliation of microbial membranes
title Engineering monolayer poration for rapid exfoliation of microbial membranes
title_full Engineering monolayer poration for rapid exfoliation of microbial membranes
title_fullStr Engineering monolayer poration for rapid exfoliation of microbial membranes
title_full_unstemmed Engineering monolayer poration for rapid exfoliation of microbial membranes
title_short Engineering monolayer poration for rapid exfoliation of microbial membranes
title_sort engineering monolayer poration for rapid exfoliation of microbial membranes
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5369539/
https://www.ncbi.nlm.nih.gov/pubmed/28451250
http://dx.doi.org/10.1039/c6sc02925f
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