Analysis of Antimicrobial-Triggered Membrane Depolarisation 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...
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Online Access: | http://journal.frontiersin.org/Journal/10.3389/fcell.2016.00029/full |
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doaj-0e4b323298564a338586d38feb65b1a92020-11-24T21:40:50ZengFrontiers Media S.A.Frontiers in Cell and Developmental Biology2296-634X2016-04-01410.3389/fcell.2016.00029192007Analysis of Antimicrobial-Triggered Membrane Depolarisation Using Voltage Sensitive DyesJ. Derk te Winkel0Declan A. Gray1Kenneth H. Seistrup2Leendert W. Hamoen3Henrik eStrahl4Newcastle UniversityNewcastle UniversityNewcastle UniversityUniversity of AmsterdamNewcastle UniversityThe 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.http://journal.frontiersin.org/Journal/10.3389/fcell.2016.00029/fullantimicrobialantimicrobial peptidesmembrane potentialvoltage-sensitive dyeDepolarizationpotentiometric dye |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
J. Derk te Winkel Declan A. Gray Kenneth H. Seistrup Leendert W. Hamoen Henrik eStrahl |
spellingShingle |
J. Derk te Winkel Declan A. Gray Kenneth H. Seistrup Leendert W. Hamoen Henrik eStrahl Analysis of Antimicrobial-Triggered Membrane Depolarisation Using Voltage Sensitive Dyes Frontiers in Cell and Developmental Biology antimicrobial antimicrobial peptides membrane potential voltage-sensitive dye Depolarization potentiometric dye |
author_facet |
J. Derk te Winkel Declan A. Gray Kenneth H. Seistrup Leendert W. Hamoen Henrik eStrahl |
author_sort |
J. Derk te Winkel |
title |
Analysis of Antimicrobial-Triggered Membrane Depolarisation Using Voltage Sensitive Dyes |
title_short |
Analysis of Antimicrobial-Triggered Membrane Depolarisation Using Voltage Sensitive Dyes |
title_full |
Analysis of Antimicrobial-Triggered Membrane Depolarisation Using Voltage Sensitive Dyes |
title_fullStr |
Analysis of Antimicrobial-Triggered Membrane Depolarisation Using Voltage Sensitive Dyes |
title_full_unstemmed |
Analysis of Antimicrobial-Triggered Membrane Depolarisation Using Voltage Sensitive Dyes |
title_sort |
analysis of antimicrobial-triggered membrane depolarisation using voltage sensitive dyes |
publisher |
Frontiers Media S.A. |
series |
Frontiers in Cell and Developmental Biology |
issn |
2296-634X |
publishDate |
2016-04-01 |
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. |
topic |
antimicrobial antimicrobial peptides membrane potential voltage-sensitive dye Depolarization potentiometric dye |
url |
http://journal.frontiersin.org/Journal/10.3389/fcell.2016.00029/full |
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