| Literature DB >> 35771433 |
Chad A Lerner1,2, Akos A Gerencser3,4.
Abstract
The mitochondrial membrane potential (ΔψM) is the major component of the bioenergetic driving force responsible for most cellular ATP produced, and it controls a host of biological processes. In intact cells, assay readouts with commonly used fluorescence ΔψM probes are distorted by factors other than ΔψM. Here, we describe a protocol to calculate both ΔψM and plasma membrane potential (ΔψP) in absolute millivolts in intact single cells, or in populations of adherent, cultured cells. Our approach generates unbiased data that allows comparison of ΔψM between cell types with different geometry and ΔψP, and to follow ΔψM in time when ΔψP fluctuates. The experimental paradigm results in fluorescence microscopy time courses using a pair of cationic and anionic probes with internal calibration points that are subsequently computationally converted to millivolts on an absolute scale. The assay is compatible with wide field, confocal or two-photon microscopy. The method given here is optimized for a multiplexed, partial 96-well microplate format to record ΔψP and ΔψM responses for three consecutive treatment additions.Entities:
Keywords: Bis-oxonol; Cell culture; Cellular heterogeneity; Fluorescence microscopy; Live cell microscopy; MitoTracker; Mitochondrial biogenesis; Mitochondrial membrane potential; Plasma membrane potential; Single cell; TMRM; Tetramethylrhodamine methyl ester
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Year: 2022 PMID: 35771433 PMCID: PMC9377305 DOI: 10.1007/978-1-0716-2309-1_2
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745