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Analysis of Antimicrobial-Triggered Membrane Depolarization Using Voltage Sensitive Dyes
The bacterial cytoplasmic membrane is a major inhibitory target for antimicrobial compounds. Commonly, although not exclusively, these compounds unfold their antimicrobial activity by disrupting the essential barrier function of the cell membrane. As a consequence, membrane permeability assays are c...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4829611/ https://www.ncbi.nlm.nih.gov/pubmed/27148531 http://dx.doi.org/10.3389/fcell.2016.00029 |
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author | te Winkel, J. Derk Gray, Declan A. Seistrup, Kenneth H. Hamoen, Leendert W. Strahl, Henrik |
author_facet | te Winkel, J. Derk Gray, Declan A. Seistrup, Kenneth H. Hamoen, Leendert W. Strahl, Henrik |
author_sort | te Winkel, J. Derk |
collection | PubMed |
description | The bacterial cytoplasmic membrane is a major inhibitory target for antimicrobial compounds. Commonly, although not exclusively, these compounds unfold their antimicrobial activity by disrupting the essential barrier function of the cell membrane. As a consequence, membrane permeability assays are central for mode of action studies analysing membrane-targeting antimicrobial compounds. The most frequently used in vivo methods detect changes in membrane permeability by following internalization of normally membrane impermeable and relatively large fluorescent dyes. Unfortunately, these assays are not sensitive to changes in membrane ion permeability which are sufficient to inhibit and kill bacteria by membrane depolarization. In this manuscript, we provide experimental advice how membrane potential, and its changes triggered by membrane-targeting antimicrobials can be accurately assessed in vivo. Optimized protocols are provided for both qualitative and quantitative kinetic measurements of membrane potential. At last, single cell analyses using voltage-sensitive dyes in combination with fluorescence microscopy are introduced and discussed. |
format | Online Article Text |
id | pubmed-4829611 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-48296112016-05-04 Analysis of Antimicrobial-Triggered Membrane Depolarization Using Voltage Sensitive Dyes te Winkel, J. Derk Gray, Declan A. Seistrup, Kenneth H. Hamoen, Leendert W. Strahl, Henrik Front Cell Dev Biol Physiology The bacterial cytoplasmic membrane is a major inhibitory target for antimicrobial compounds. Commonly, although not exclusively, these compounds unfold their antimicrobial activity by disrupting the essential barrier function of the cell membrane. As a consequence, membrane permeability assays are central for mode of action studies analysing membrane-targeting antimicrobial compounds. The most frequently used in vivo methods detect changes in membrane permeability by following internalization of normally membrane impermeable and relatively large fluorescent dyes. Unfortunately, these assays are not sensitive to changes in membrane ion permeability which are sufficient to inhibit and kill bacteria by membrane depolarization. In this manuscript, we provide experimental advice how membrane potential, and its changes triggered by membrane-targeting antimicrobials can be accurately assessed in vivo. Optimized protocols are provided for both qualitative and quantitative kinetic measurements of membrane potential. At last, single cell analyses using voltage-sensitive dyes in combination with fluorescence microscopy are introduced and discussed. Frontiers Media S.A. 2016-04-13 /pmc/articles/PMC4829611/ /pubmed/27148531 http://dx.doi.org/10.3389/fcell.2016.00029 Text en Copyright © 2016 te Winkel, Gray, Seistrup, Hamoen and Strahl. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Physiology te Winkel, J. Derk Gray, Declan A. Seistrup, Kenneth H. Hamoen, Leendert W. Strahl, Henrik Analysis of Antimicrobial-Triggered Membrane Depolarization Using Voltage Sensitive Dyes |
title | Analysis of Antimicrobial-Triggered Membrane Depolarization Using Voltage Sensitive Dyes |
title_full | Analysis of Antimicrobial-Triggered Membrane Depolarization Using Voltage Sensitive Dyes |
title_fullStr | Analysis of Antimicrobial-Triggered Membrane Depolarization Using Voltage Sensitive Dyes |
title_full_unstemmed | Analysis of Antimicrobial-Triggered Membrane Depolarization Using Voltage Sensitive Dyes |
title_short | Analysis of Antimicrobial-Triggered Membrane Depolarization Using Voltage Sensitive Dyes |
title_sort | analysis of antimicrobial-triggered membrane depolarization using voltage sensitive dyes |
topic | Physiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4829611/ https://www.ncbi.nlm.nih.gov/pubmed/27148531 http://dx.doi.org/10.3389/fcell.2016.00029 |
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