用对接和分子动力学方法检测持久性有机污染物与雄激素受体配体结合域的结合模式

Q3 Biochemistry, Genetics and Molecular Biology BMC Structural Biology Pub Date : 2013-09-22 DOI:10.1186/1472-6807-13-16
Xian Jin Xu, Ji Guo Su, Anna Rita Bizzarri, Salvatore Cannistraro, Ming Liu, Yi Zeng, Wei Zu Chen, Cun Xin Wang
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引用次数: 7

摘要

持久性有机污染物(POPs)在工业化合物、燃烧产物或农药释放后,在环境中持续存在。接触持久性有机污染物与各种生殖障碍有关,例如精液质量下降、睾丸癌和性别比失衡。在持久性有机污染物中,二氯二苯二氯乙烯(4,4 ' -DDE)和多氯联苯(PCBs)是分布最广、研究最充分的化合物。近年来的研究表明,4,4 ' -DDE是雄激素受体(AR)的拮抗剂。然而,这种抑制的机制尚不清楚。CB-153是多氯联苯最常见的同系物,而CB-153对AR的作用仍在争论中。采用分子对接和分子动力学(MD)方法研究了4,4 ' -DDE和CB-153对AR配体结合域(LBD)的结合方式和抑制机制。已经检测和分析了几个潜在的结合位点。一个可能的结合位点是AR天然配体雄激素5α-二氢睾酮(DHT)的相同结合位点。另一个位于配体依赖性转录激活功能(AF2)区域,该区域对共激活剂的募集至关重要。此外,还发现了与受体结合自由能较低的持久性有机污染物可能存在的新的结合位点。配体和受体之间的详细相互作用已被描述。讨论了持久性有机污染物对AR的干扰机理。POPs通过结合AR/LBD上的三个可能的结合位点破坏AR的功能。其中一个与AR天然配体的结合位点相同,另一个位于AF2区。第三个位于受体n端附近的间隙中。值得注意的是,持久性有机污染物与AR/LBD的结合自由能值与天然配体雄激素DHT相当。
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Detection of persistent organic pollutants binding modes with androgen receptor ligand binding domain by docking and molecular dynamics

Persistent organic pollutants (POPs) are persistent in the environment after release from industrial compounds, combustion productions or pesticides. The exposure of POPs has been related to various reproductive disturbances, such as reduced semen quality, testicular cancer, and imbalanced sex ratio. Among POPs, dichlorodiphenyldichloroethylene (4,4’-DDE) and polychlorinated biphenyls (PCBs) are the most widespread and well-studied compounds. Recent studies have revealed that 4,4’-DDE is an antagonist of androgen receptor (AR). However, the mechanism of the inhibition remains elusive. CB-153 is the most common congener of PCBs, while the action of CB-153 on AR is still under debate.

Molecular docking and molecular dynamics (MD) approaches have been employed to study binding modes and inhibition mechanism of 4,4’-DDE and CB-153 against AR ligand binding domain (LBD). Several potential binding sites have been detected and analyzed. One possible binding site is the same binding site of AR natural ligand androgen 5α-dihydrotestosterone (DHT). Another one is on the ligand-dependent transcriptional activation function (AF2) region, which is crucial for the co-activators recruitment. Besides, a novel possible binding site was observed for POPs with low binding free energy with the receptor. Detailed interactions between ligands and the receptor have been represented. The disrupting mechanism of POPs against AR has also been discussed.

POPs disrupt the function of AR through binding to three possible biding sites on AR/LBD. One of them shares the same binding site of natural ligand of AR. Another one is on AF2 region. The third one is in a cleft near N-terminal of the receptor. Significantly, values of binding free energy of POPs with AR/LBD are comparable to that of natural ligand androgen DHT.

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来源期刊
CiteScore
3.60
自引率
0.00%
发文量
0
审稿时长
>12 weeks
期刊介绍: BMC Structural Biology is an open access, peer-reviewed journal that considers articles on investigations into the structure of biological macromolecules, including solving structures, structural and functional analyses, and computational modeling.
期刊最新文献
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