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Affinity Purification Using Recombinant PXR as a Tool to Characterize Environmental Ligands

机译:使用重组PXR作为表征环境配体的工具进行亲和纯化

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摘要

Many environmental endocrine disrupting compounds act as ligands for nuclear receptors. The human pregnane X receptor (hPXR), for instance, is activated by a variety of environmental ligands such as steroids, pharmaceutical drugs, pesticides, alkylphenols, polychlorinated biphenyls and polybromo diethylethers. Some of us have previously reported the occurrence of hPXR ligands in environmental samples but failed to identify them. The aim of this study was to test whether a PXR-affinity column, in which recombinant hPXR was immobilized on solid support, could help the purification of these chemicals. Using PXR ligands of different affinity (10 nM < EC50 < 10 μM), we demonstrated that the PXR-affinity preferentially column captured ligands with medium to high affinities (EC50 < 1 μM). Furthermore, by using the PXR-affinity column to analyze an environmental sample containing ERa, AhR, AR, and PXR activities, we show that (ⅰ) half of the PXR activity of the sample was due to compounds with medium to high affinity for PXR and (ⅱ) PXR shared ligands with ERa, AR, and AhR. These findings demonstrate that the newly developed PXR-affinity column coupled to reporter cell lines represents a valuable tool for the characterization of the nature of PXR active compounds and should therefore guide and facilitate their further analysis.
机译:许多破坏环境内分泌的化合物充当核受体的配体。例如,人类孕烷X受体(hPXR)被多种环境配体激活,如类固醇,药物,农药,烷基酚,多氯联苯和多溴二乙醚。我们中有些人以前曾报道过hPXR配体在环境样品中的发生,但未能鉴定出它们。这项研究的目的是测试将重组hPXR固定在固体支持物上的PXR亲和柱是否可以帮助纯化这些化学物质。使用不同亲和力(10 nM <EC50 <10μM)的PXR配体,我们证明PXR亲和力优先捕获了中等至高亲和力(EC50 <1μM)的配体。此外,通过使用PXR亲和柱分析包含ERa,AhR,AR和PXR活性的环境样品,我们显示出样品的PXR活性的一半是由于对PXR具有中等至高亲和力的化合物所致(ⅱ)PXR与ERa,AR和AhR共享配体。这些发现表明,新近开发的与报告细胞系偶联的PXR亲和柱代表了表征PXR活性化合物性质的宝贵工具,因此应指导并促进其进一步的分析。

著录项

  • 来源
    《Environmental toxicology》 |2014年第2期|207-215|共9页
  • 作者单位

    IRCM, Institut de Recherche en Cancerologie de Montpellier, CRLC Val d'Aurelle Paul Lamarque, INSERM, U896 34298 Montpellier, France,Universite Montpellier 1, 34298 Montpellier, France,UMR 5569 Hydrosciences, Universite Montpellier I, 34060 Montpellier, France,U.S. EPA, Office of Research and Development, National Exposure Research Laboratory, Research Triangle Park, NC 27 711, USA;

    IRCM, Institut de Recherche en Cancerologie de Montpellier, CRLC Val d'Aurelle Paul Lamarque, INSERM, U896 34298 Montpellier, France,Universite Montpellier 1, 34298 Montpellier, France;

    IRCM, Institut de Recherche en Cancerologie de Montpellier, CRLC Val d'Aurelle Paul Lamarque, INSERM, U896 34298 Montpellier, France,Universite Montpellier 1, 34298 Montpellier, France;

    UMR 1089 Xenobiotiques, INRA, F-31931 Toulouse, France;

    Institut National de I'Environnement Industriels et des Risques (INERIS), Unite Ecotoxicologie in vitro et in vivo f-60550 Verneuil-en-Halatte, France;

    IRCM, Institut de Recherche en Cancerologie de Montpellier, CRLC Val d'Aurelle Paul Lamarque, INSERM, U896 34298 Montpellier, France,Universite Montpellier 1, 34298 Montpellier, France;

    UMR 5569 Hydrosciences, Universite Montpellier I, 34060 Montpellier, France;

    IRCM, Institut de Recherche en Cancerologie de Montpellier, CRLC Val d'Aurelle Paul Lamarque, INSERM, U896 34298 Montpellier, France,Universite Montpellier 1, 34298 Montpellier, France;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    PXR; ERa; AhR; AR; affinity column;

    机译:PXR;时代;AhR;AR;亲和力专栏;

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