Binding interactions of halogenated bisphenol A with mouse PPAR alpha: In vitro investigation and molecular dynamics simulation
文献类型: 外文期刊
作者: Zhang, Jie 1 ; Li, Tiezhu 1 ; Wang, Tuoyi 1 ; Guan, Tianzhu 2 ; Yu, Hansong 3 ; Li, Zhuolin 1 ; Wang, Yongzhi 1 ; Wang, Y 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
关键词: Fluorescence polarization;Electrostatic potential;Molecular docking;Halogenated bisphenol A;Peroxisome proliferator-activated receptor alpha
期刊名称:TOXICOLOGY LETTERS ( 影响因子:4.372; 五年影响因子:4.372 )
ISSN: 0378-4274
年卷期: 2018 年 283 卷
页码:
收录情况: SCI
摘要: The binding of bisphenol A (BPA) and its halogenated derivatives (halogenated BPAs) to mouse peroxisome proliferator-activated receptor alpha ligand binding domain (mPPAR alpha-LBD) was examined by a combination of in vitro investigation and in silico simulation. Fluorescence polarization (FP) assay showed that halogenated BPAs could bind to mPPAR alpha-LBD* as the affinity ligands. The calculated electrostatic potential (ESP) illustrated the different charge distributions of halogenated BPAs with altered halogenation patterns. As electron-attracting substituents, halogens decrease the positive electrostatic potential and thereby have a significant influence on the electrostatic interactions of halogenated BPAs with mPPAR alpha-LBD*. The docking results elucidated that hydrophobic and hydrogen-bonding interactions may also contribute to stabilize the binding of the halogenated BPAs to their receptor molecule. Comparison of the calculated binding energies with the experimentally determined affinities yielded a good correlation (R-2 = 0.6659) that could provide a rational basis for designing environmentally benign chemicals with reduced toxicities. This work can potentially be used for preliminary screening of halogenated BPAs.
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