vitamin-k-semiquinone-radical and 3-((3-cholamidopropyl)dimethylammonium)-1-propanesulfonate

vitamin-k-semiquinone-radical has been researched along with 3-((3-cholamidopropyl)dimethylammonium)-1-propanesulfonate* in 2 studies

Other Studies

2 other study(ies) available for vitamin-k-semiquinone-radical and 3-((3-cholamidopropyl)dimethylammonium)-1-propanesulfonate

ArticleYear
Characterization and partial purification of microsomal NAD(P)H:quinone oxidoreductases.
    Archives of biochemistry and biophysics, 2000, Mar-01, Volume: 375, Issue:1

    Quinone oxidoreductases are flavoproteins that catalyze two-electron reduction and detoxification of quinones. This leads to the protection of cells against toxicity, mutagenicity, and cancer due to exposure to environmental and synthetic quinones and its precursors. Two cytosolic forms of quinone oxidoreductases [NAD(P)H:quinone oxidoreductase 1 (NQO1) and NRH:quinone oxidoreductase 2 (NQO2)] were previously identified, purified, and cloned. A role of cytosolic NQO1 in protection of cells from oxidative stress, cytotoxicity, and mutagenicity of quinones was established. Currently, we have characterized and partially purified the NQO activity from rat liver microsomes. This activity was designated as microsomal NQO (mNQO). The mNQO activity showed significantly higher affinity for NADH than NADPH as electron donors and catalyzed reduction of 2,6-dichlorophenolindophenol and menadione. The mNQO activity was insensitive to dicoumarol, a potent inhibitor of cytosolic NQO1. Western analysis of microsomal proteins revealed 29- and 18-kDa bands that cross-reacted with polyclonal antibodies raised against cytosolic NQO1. The mNQO activity was partially purified by solubilization of microsomes with detergent Chaps, ammonium sulfate fractionation, and DEAE-Sephacel column chromatography. The microsomal mNQO proteins are expected to provide additional protection after cytosolic NQOs against quinone toxicity and mutagenicity.

    Topics: 2,6-Dichloroindophenol; Animals; Cholic Acids; Chromatography, Ion Exchange; Cytosol; Detergents; Dicumarol; Enzyme Activation; Enzyme Inhibitors; Fractional Precipitation; Immune Sera; Isoenzymes; Microsomes, Liver; Molecular Weight; NAD; NAD(P)H Dehydrogenase (Quinone); NADP; p-Chloromercuribenzoic Acid; Rats; Rats, Inbred F344; Sulfhydryl Reagents; Vitamin K

2000
A new detergent for the solubilization of the vitamin K-dependent carboxylation system from liver microsomes: comparison with triton X-100.
    Analytical biochemistry, 1982, Volume: 121, Issue:2

    Topics: Animals; Cholic Acids; Detergents; Ligases; Male; Microsomes, Liver; Octoxynol; Polyethylene Glycols; Rats; Rats, Inbred Strains; Solubility; Surface-Active Agents; Vitamin K; Vitamin K Deficiency

1982