| Literature DB >> 34099175 |
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.Entities:
Keywords: Electrophysiology; FLIM; Fluorescence lifetime; Imaging; Membrane potential; Microscopy; Voltage-sensitive fluorophore
Mesh:
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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