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Fast steroid hormone metabolism assays with electrochemical liver microsomal bioreactor based on polydopamine encapsulated gold-graphene nanocomposite

机译:基于聚二胺封装金石墨烯纳米复合材料的基于聚二胺的电化学肝微粒体生物反应器快速类固醇激素代谢测定

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摘要

The metabolites of steroid hormones catalyzed by cytochrome P450s (CYPs) play a significant role in carcinogenicity. Herein we report a facile electrochemical liver microsomal bioreactor based on the polydopamine encapsulated gold-graphene nanocomposite (PDA/Au@RGO) for the fast steroid hormone metabolism assays. In this work, human liver microsomes (HLMs) were directly attached on PDA/Au@RGO without any activation process. Besides, due to the high conductivity, large active areas and good biocompatibility of PDA/Au@RGO, the direct electron transfer of HLM with the rate constant (k(s)) of 8.9 s(-1) was achieved and the bioactivity of membrane bound proteins in HLM was largely maintained. Compared with recombinant enzymes, the immobilized HLM displayed obviously lower apparent Michaelis-Menten constant (K-m(app)) of 175 +/- 20 mu M. Through HPLC-MS and CYP-specific inhibition experiment, the electrode-driven catalytic behavior of HLM for the conversion of testosterone to 6 beta-OH-testosterone was confirmed. Moreover, the constructed HLM bioreactor was also successfully applied to the metabolism of other two steroid hormones (estrone and progesterone). This work has immense significance in the design of practically viable HLM bioreactors for the toxicity analysis of steroid hormones and stereoselective metabolite synthesis. (C) 2017 Elsevier Ltd. All rights reserved.
机译:细胞色素P450s(CYPS)催化的类固醇激素代谢物在致癌性中起重要作用。在此,我们报告了基于聚二氨基氨基封装的金 - 石墨烯纳米复合材料(PDA / Au @ Rgo)的容易电化学肝微粒体生物反应器,用于快速类固醇激素代谢测定。在这项工作中,人肝微粒体(HLMS)直接连接在PDA / Au @ Rgo上,没有任何激活过程。此外,由于高导电性,大型活性区域和PDA / Au @ Rgo的良好生物相容性,实现了8.9 s(-1)速率常数(k(-1)的HLM的直接电子转移和生物活性在很大程度上维持HLM中的膜结合蛋白。与重组酶相比,固定化的HLM显示出明显的明显下表观迈克莱斯 - Menten常数(KM(APP)),通过HPLC-MS和CYP特异性抑制实验,HLM的电极驱动催化行为为了将睾酮转化为6β-OH-睾酮。此外,构建的HLM生物反应器也成功地应用于其他两种类固醇激素(雌激素和孕酮)的代谢。这项工作在实际上可行的HLM生物反应器设计方面具有巨大意义,用于类固醇激素和立体选择性代谢物合成的毒性分析。 (c)2017 Elsevier Ltd.保留所有权利。

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