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Metabolism of Vitamin D2 to 17,20,24-Trihydroxyvitamin D2 by Cytochrome P450scc (CYP11A1)

机译:细胞色素将维生素D2代谢为17,20,24-三羟基维生素D2 P450scc(CYP11A1)

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摘要

As well as catalyzing the conversion of cholesterol to pregnenolone for steroid synthesis, cytochrome P450scc (P450scc) can also metabolize vitamins D2 (D2) and D3 (D3). Two products of D2 metabolism by P450scc, 20-hydroxyvitamin D2 and 17,20-dihydroxyvitamin D2, have been identified and shown to exert biological activity on cultured keratinocytes. The aim of this study was to fully characterize the metabolism of D2 by P450scc, including identifying additional products and determining the kinetics of D2 metabolism. Two new products were isolated by reverse-phase high-performance liquid chromatography: a dihydroxy metabolite with a hydroxyl group at C20 plus another unidentified position, and a trihydroxy metabolite identified by NMR as 17,20,24-trihydroxyvitamin D2. Kinetics of D2 metabolism was determined with substrate solubilized by 2-hydroxypropyl-β-cyclodextrin or incorporated into phospholipid vesicles. In 2-hydroxypropyl-β-cyclodextrin, D2 was hydroxylated at C20 with a kcat/Km 5-fold lower than that for cholesterol metabolism. 20-Hydroxyvitamin D2 was hydroxylated with a similar kcat/Km to D2, whereas 17,20-dihydroxyvitamin D2 was hydroxylated with a lower kcat/Km than that for D2 in 2-hydroxypropyl-β-cyclodextrin. In vesicles, D2 displayed a high Km relative to that for cholesterol, but hydroxylation resulted in products that could be further hydroxylated with relatively low Km values. We conclude that P450scc catalyzes three sequential hydroxylations of D2 producing 20-hydroxyvitamin D2, 17,20-dihydroxyvitamin D2, and 17,20,24-trihydroxyvitamin D2, which dissociate from the active site of P450scc and accumulate in the reaction mixture. D2 metabolism occurs with lower efficiency (kcat/Km) than that observed for both cholesterol and D3 metabolism by P450scc.
机译:细胞色素P450scc(P450scc)不仅可以催化胆固醇转换为孕烯醇酮来合成甾体,还可以代谢维生素D2(D2)和D3(D3)。已鉴定出P450scc的D2代谢的两种产物20-羟基维生素D2和17,20-二羟基维生素D2,它们显示出对培养的角质形成细胞具有生物学活性。这项研究的目的是全面表征P450scc对D2的代谢,包括鉴定其他产物并确定D2代谢的动力学。通过反相高效液相色谱法分离了两种新产物:在C20处带有羟基的另一个二羟基代谢物加上另一个未确定的位置,以及通过NMR鉴定为17,20,24-三羟基维生素D2的三羟基代谢物。用2-羟丙基-β-环糊精溶解或掺入磷脂囊泡的底物测定D2代谢的动力学。在2-羟丙基-β-环糊精中,D2在C20处被羟化,其kcat / Km比胆固醇代谢的kcat / Km低5倍。在2-羟丙基-β-环糊精中,以与D2相似的kcat / Km羟基化20-羟基维生素D2,而以比D2更低的kcat / Km羟基化17,20-二羟基维生素D2。在囊泡中,相对于胆固醇而言,D2表现出较高的Km,但羟基化导致产物可以以相对较低的Km值进一步被羟基化。我们得出的结论是,P450scc催化D2的三个连续羟基化,从而生成20-羟基维生素D2、17,20-二羟基维生素D2和17,20,24-三羟基维生素D2,它们从P450scc的活性位点解离并积聚在反应混合物中。 D2代谢发生的效率(kcat / Km)要比P450scc观察到的胆固醇和D3代谢的效率低。

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