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

Methods Enzymol

Department of Chemistry, University of California, Berkeley, CA, United States; Department of Molecular & Cell Biology, University of California, Berkeley, CA, United States; Helen Wills Neuroscience Institute, University of California, Berkeley, CA, United States. Electronic address:

Published: June 2021

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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8356362PMC
http://dx.doi.org/10.1016/bs.mie.2021.02.009DOI Listing

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