INACTIVATION OF ESCHERICHIA-COLI EXPRESSED RABBIT CYTOCHROME-P-450 2CENZYMES BY 17-BETA-SUBSTITUTED STEROIDS

Citation
Pa. Klekotka et al., INACTIVATION OF ESCHERICHIA-COLI EXPRESSED RABBIT CYTOCHROME-P-450 2CENZYMES BY 17-BETA-SUBSTITUTED STEROIDS, The Journal of pharmacology and experimental therapeutics, 274(3), 1995, pp. 1450-1455
Citations number
23
Categorie Soggetti
Pharmacology & Pharmacy
ISSN journal
00223565
Volume
274
Issue
3
Year of publication
1995
Pages
1450 - 1455
Database
ISI
SICI code
0022-3565(1995)274:3<1450:IOEERC>2.0.ZU;2-W
Abstract
The specific inactivation of rabbit cytochromes P-450 2C by 17 beta-su bstituted steroids has been investigated by using purified, Escherichi a coil-expressed enzymes. The expressed P-450s provided a means to cha racterize accurately the effects of 21,21-dichloroprogesterone, 21,21- dichloropregnenolone, 21-chloro-21-fluoropregnenolone, pregn-5,20-dien e-3 beta-ol and pregn-4,20-diene-3-one on progesterone hydroxylation b y P-450 2C5, 2C4, 2C3 and 2C3v. Previous studies using rabbit liver mi crosomes had suggested that 21-chloro-21-fluoropregnenolone is a selec tive inactivator of 2C5, a progesterone 21-hydroxylase. Studies of the expressed P-450 2C forms showed little selectivity of 21,21-dichlorop rogesterone, pregn-5,20-diene-3 beta-ol or pregn-4,20-diene-3-one, whe reas 21,21-dichloropregnenolone and 21-chloro-21-fluoropregnenolone pr eferentially inactivate 2C5. The data indicate the importance of proge sterone 21-hydroxylase activity in facilitating selective mechanism-ba sed inactivation of 2C subfamily P-450s by 21,21-dihalogenated steroid s. Studies of the inactivation of P-450 2C16, a progesterone 16 alpha- hydroxylase, by the three dihalogenated steroids yielded results consi stent with previous findings of 16 alpha-hydroxylase inactivation in r abbit liver microsomes from the inbred B/J strain. Additionally, two m utants, 2C3v:V113A and 2C3v:V113A,T364N were created which confer prog esterone 21-hydroxylation on 2C3v. The single mutant, a 6 beta- and 21 -hydroxylase, is inactivated rapidly by all three of the 21,21-dihalog enated steroids, whereas the double mutant, a 16 alpha- and el-hydroxy lase, is preferentially inactivated by 21,21-dichloroprogesterone. The se results further support the importance of residues 364 and 113 in r abbit 2C enzymes for conferring not only progesterone 16 alpha-, 6 bet a- or 21-hydroxylase activity, but also susceptibility to inactivation by el-halogenated progesterone and pregnenolone derivatives.