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Estrogenicity of halogenated bisphenol A: in vitro and in silico investigations

文献类型： 外文期刊

作者： Zhang, Jie 1 ; Li, Tiezhu 1 ; Wang, Tuoyi 1 ; Yuan, Cuiping 1 ; Zhong, Shuning 2 ; Guan, Tianzhu 2 ; Li, Zhuolin 1 ; Wang 1 ;

作者机构： 1.Jilin Acad Agr Sci, Inst Agr Resources & Environm, Changchun 130033, Jilin, Peoples R China

2.Jilin Univ, Coll Food Sci & Engn, Changchun 130062, Jilin, Peoples R China

3.Jilin Agr Univ, Coll Food Sci & Engn, Changchun 130118, Jilin, Peoples R China

4.Jilin Univ, Coll Chem, State Key Lab Supramol Struct & Mat, Chang

关键词： Halogenated bisphenol A; Estrogen receptor alpha; Fluorescence polarization; Molecular modeling

期刊名称：ARCHIVES OF TOXICOLOGY （ 影响因子：5.153； 五年影响因子：6.352 ）

ISSN： 0340-5761

年卷期： 2018 年 92 卷 3 期

页码：

收录情况： SCI

摘要： The binding interactions of bisphenol A (BPA) and its halogenated derivatives (halogenated BPAs) to human estrogen receptor alpha ligand binding domain (hER alpha-LBD) was investigated using a combined in vitro and in silico approach. First, the recombinant hER alpha-LBD was prepared as a soluble protein in Escherichia coli BL21(DE3)pLysS. A native fluorescent phytoestrogen, coumestrol, was employed as tracer for the fluorescence polarization assay. The results of the in vitro binding assay showed that bisphenol compounds could bind to hER alpha-LBD as the affinity ligands. All the tested halogenated BPAs exhibited weaker receptor binding than BPA, which might be explained by the steric effect of substituents. Molecular docking studies elucidated that the halogenated BPAs adopted different conformations in the flexible hydrophobic ligand binding pocket (LBP), which is mainly dependent on their distinct halogenation patterns. The compounds with halogen substituents on the phenolic rings and on the bridging alkyl moiety acted as agonists and antagonists for hER alpha, respectively. Interestingly, all the compounds in the agonist conformation of hER alpha formed a hydrogen bond with His524, while the compounds in the antagonist conformation formed a hydrogen bond with Thr347. These docking results suggested a pivotal role of His524/Thr347 in maintaining the hER alpha structure in the biologically active agonist/antagonist conformation. Comparison of the calculated binding energies vs. experimental binding affinities yielded a good correlation, which might be applicable for the structure-based design of novel bisphenol compounds with reduced toxicities and for environmental risk assessment. In addition, based on hER alpha-LBD as a recognition element, the proposed fluorescence polarization assay may offer an alternative to chromatographic techniques for the multi-residue determination of bisphenol compounds.

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