digitonin and triphenylmethylphosphonium

digitonin has been researched along with triphenylmethylphosphonium* in 2 studies

Other Studies

2 other study(ies) available for digitonin and triphenylmethylphosphonium

ArticleYear
Use of digitonin fractionation to determine mitochondrial transmembrane ion distribution in cells during anoxia.
    Analytical biochemistry, 1985, Volume: 146, Issue:1

    A method to determine intracellular distribution of ions and metabolites under conditions of low oxygen concentration was developed. The technique involves rapid digitonin fractionation and addition of cyanide to inhibit reoxygenation. Applicability of the procedure was examined by studying the distribution of the lipophilic ion triphenylmethylphosphonium, the weak acid 5,5-dimethyloxazolidine-2,4-dione, and adenine nucleotides.

    Topics: Adenine Nucleotides; Animals; Cell Fractionation; Digitonin; Dimethadione; Hydrogen-Ion Concentration; Hypoxia; Ions; Male; Membrane Potentials; Mitochondria, Liver; Onium Compounds; Oxygen Consumption; Rats; Trityl Compounds

1985
Characterization of a rapid cellular-fractionation technique for hepatocytes. Application in the measurement of mitochondrial membrane potential in situ.
    The Biochemical journal, 1984, Apr-15, Volume: 219, Issue:2

    A rapid cellular-fractionation technique [ Hoek , Nicholls & Williamson (1980) J. Biol. Chem. 255, 1458-1464] was further characterized by using hepatocytes. Of the mitochondrial marker-enzyme activity, 80% was routinely separated from 71-98% of the total cell activities of marker enzymes for plasma membranes, Golgi-membranes, endoplasmic reticulum, lysosomes and cytosol. The mitochondria were contaminated with 53% of cell nuclei. [3H]Triphenylmethylphosphonium ion (TPMP+) was added to hepatocytes in an attempt to measure cellular transmembrane electrical potentials. After rapid cell fractionation the electrical potential between mitochondria in situ and the incubation medium was found to be 202 mV. This value was slightly increased when hepatocytes were treated with oligomycin, but substantially decreased by oligomycin plus an uncoupler of oxidative phosphorylation. Although estimates of TPMP+ binding were obtained, substantial difficulties prevented the accurate measurement of the electrical potential across the plasma membrane. It is concluded that TPMP+ may be employed to demonstrate the integrity of mitochondria during the fractionation procedures. However, the cation is inadequate for the determination of the separate components of the electrical potential between the mitochondrial matrix and the incubation medium.

    Topics: Animals; Cell Fractionation; Digitonin; Intracellular Membranes; Kinetics; Liver; Male; Membrane Potentials; Mitochondria, Liver; Onium Compounds; Rats; Rats, Inbred Strains; Trityl Compounds; Valinomycin

1984