Literature DB >> 34099175

VoltageFluor dyes and fluorescence lifetime imaging for optical measurement of membrane potential.

Anneliese M M Gest1, Susanna K Yaeger-Weiss1, Julia R Lazzari-Dean1, Evan W Miller2.   

Abstract

Membrane potential is a fundamental biophysical parameter common to all of cellular life. Traditional methods to measure membrane potential rely on electrodes, which are invasive and low-throughput. Optical methods to measure membrane potential are attractive because they have the potential to be less invasive and higher throughput than classic electrode based techniques. However, most optical measurements rely on changes in fluorescence intensity to detect changes in membrane potential. In this chapter, we discuss the use of fluorescence lifetime imaging microscopy (FLIM) and voltage-sensitive fluorophores (VoltageFluors, or VF dyes) to estimate the millivolt value of membrane potentials in living cells. We discuss theory, application, protocols, and shortcomings of this approach.
Copyright © 2021 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Electrophysiology; FLIM; Fluorescence lifetime; Imaging; Membrane potential; Microscopy; Voltage-sensitive fluorophore

Mesh:

Substances:

Year:  2021        PMID: 34099175      PMCID: PMC8356362          DOI: 10.1016/bs.mie.2021.02.009

Source DB:  PubMed          Journal:  Methods Enzymol        ISSN: 0076-6879            Impact factor:   1.600


  18 in total

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3.  Voltage-clamp and current-clamp recordings from mammalian DRG neurons.

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6.  Optical estimation of absolute membrane potential using fluorescence lifetime imaging.

Authors:  Julia R Lazzari-Dean; Anneliese Mm Gest; Evan W Miller
Journal:  Elife       Date:  2019-09-23       Impact factor: 8.140

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8.  The LRRC8/VRAC anion channel facilitates myogenic differentiation of murine myoblasts by promoting membrane hyperpolarization.

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Journal:  Mol Biol Cell       Date:  2014-12-01       Impact factor: 4.138

Review 10.  Targeting potassium channels in cancer.

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