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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Main Authors: J. Derk te Winkel, Declan A. Gray, Kenneth H. Seistrup, Leendert W. Hamoen, Henrik eStrahl
Format: Article
Language:English
Published: Frontiers Media S.A. 2016-04-01
Series:Frontiers in Cell and Developmental Biology
Subjects:
Online Access:http://journal.frontiersin.org/Journal/10.3389/fcell.2016.00029/full
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spelling 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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