Novel sensitive high-performance liquid chromatographic method for assay of coumarin 7-hydroxylation
Jazyk angličtina Země Nizozemsko Médium print
Typ dokumentu srovnávací studie, časopisecké články, práce podpořená grantem
PubMed
10574186
Knihovny.cz E-zdroje
- MeSH
- aromatické hydroxylasy * MeSH
- cytochrom P450 CYP2A6 MeSH
- Escherichia coli genetika MeSH
- fluorescenční spektrometrie MeSH
- hydroxylace MeSH
- jaterní mikrozomy enzymologie MeSH
- kinetika MeSH
- krysa rodu Rattus MeSH
- kumariny metabolismus MeSH
- lidé MeSH
- NADPH-cytochrom c-reduktasa metabolismus MeSH
- oxygenasy se smíšenou funkcí analýza metabolismus MeSH
- rekombinantní proteiny metabolismus MeSH
- senzitivita a specificita MeSH
- systém (enzymů) cytochromů P-450 analýza metabolismus MeSH
- vysokoúčinná kapalinová chromatografie metody MeSH
- zvířata MeSH
- Check Tag
- krysa rodu Rattus MeSH
- lidé MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- srovnávací studie MeSH
- Názvy látek
- aromatické hydroxylasy * MeSH
- coumarin MeSH Prohlížeč
- CYP2A6 protein, human MeSH Prohlížeč
- cytochrom P450 CYP2A6 MeSH
- kumariny MeSH
- NADPH-cytochrom c-reduktasa MeSH
- oxygenasy se smíšenou funkcí MeSH
- rekombinantní proteiny MeSH
- systém (enzymů) cytochromů P-450 MeSH
In this paper, a novel HPLC-based method with fluorometric detection of coumarin 7-hydroxylase is presented. The described method provides a time-effective, more sensitive and specific alternative to the previously used spectrofluorometric assay. Using the developed method, metabolism of coumarin in 11 samples of human liver microsomes was evaluated and 1790+/-690 pmol/min/nmol cytochrome P450 (CYP) activity was found. Kinetic parameters and linearity of coumarin 7-hydroxylation were studied in a reconstituted system consisting of recombinant CYP2A6 expressed in Escherichia coli, rat NADPH-CYP reductase and usual components. It was found that a 3.5 to 30 min time of incubation is suitable for estimation of coumarin 7-hydroxylase activity. Observed Km and Vmax values in the CYP2A6 reconstituted system were 1.48+/-0.37 microM and 3360+/-180 pmol product/min/nmol CYP, respectively.
In Vitro Interaction of Binuclear Copper Complexes with Liver Drug-Metabolizing Cytochromes P450
Minipig cytochrome P450 3A, 2A and 2C enzymes have similar properties to human analogs