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Identification of new probe substrates for human CYP20A1
- Source :
- Biological Chemistry. 401:361-365
- Publication Year :
- 2019
- Publisher :
- Walter de Gruyter GmbH, 2019.
-
Abstract
- CYP20A1 is a well-conserved member of the human cytochrome P450 enzyme family for which no endogenous or xenobiotic substrate is known. We have recently shown that this enzyme has moderate activity towards two proluciferin probe substrates. In order to facilitate the search for physiological substrates we have tested nine additional proluciferins in this study and identified three such probe substrates that give much higher product yields. Using one of these probes, we demonstrate inhibition of CYP20A1 activity by 1-benzylimidazole, ketoconazole and letrozole. Finally, we show that the combination of two common single nucleotide polymorphisms (SNPs) of CYP20A1 leads to an enzyme (CYP20A1Leu97Phe346) with reduced activity.
- Subjects :
- 0301 basic medicine
Clinical Biochemistry
Single-nucleotide polymorphism
Endogeny
Biochemistry
Substrate Specificity
03 medical and health sciences
chemistry.chemical_compound
0302 clinical medicine
Cytochrome P-450 Enzyme System
medicine
Humans
Molecular Biology
CYP20A1
chemistry.chemical_classification
Molecular Structure
biology
Imidazoles
Cytochrome P450
Substrate (chemistry)
Ketoconazole
030104 developmental biology
Enzyme
chemistry
030220 oncology & carcinogenesis
Letrozole
biology.protein
Xenobiotic
medicine.drug
Subjects
Details
- ISSN :
- 14374315 and 14316730
- Volume :
- 401
- Database :
- OpenAIRE
- Journal :
- Biological Chemistry
- Accession number :
- edsair.doi.dedup.....a1cbc1f3362ac91da503d98b0a6c9150
- Full Text :
- https://doi.org/10.1515/hsz-2019-0307