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Treat Alzheimer's disease by traditional Chinese medicine?

机译:用中药治疗老年痴呆症?

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Upregulated phosphodiesterase 4D (PDE4D) disrupts the regulation of calcium ion channel in the central nerve system, and hence it is considered as one of the causes of Alzheimer's disease. We employed structure-based drug design techniques and the world's largest traditional Chinese medicine (TCM) database for identifying potential TCM-based PDE4D inhibitors. We then applied multiple linear regression (MLR) and support vector machine (SVM) for quantitative structure-activity relationship model, as well as for molecular dynamics simulation analysis. Screening results suggested that metal cations, Zn2+ and Mg2+, played key roles in mediating stable protein-ligand interactions with the ligand-binding residues, Asp367 and Asp484. In addition, each ligand was shown to interfere with the active residue His326 that suggested inhibitory effects. The MLR and SVM prediction models further implied the PDE4D inhibitory effect of each TCM compound. The molecular simulation further suggested the binding stability of each compound in the PDE4D binding site. We identified three TCM compounds, such as mumefural, 2-O-feruloyl tartaric acid and kainic acid, as potential PDE4D inhibitors. In addition, we further identified the key interaction features associated with the protein-ligand-binding stabilities.View full textDownload full textKeywordstraditional Chinese medicine, docking, support vector machine, molecular dynamics, Alzheimer's diseaseRelated var addthis_config = { ui_cobrand: "Taylor & Francis Online", services_compact: "citeulike,netvibes,twitter,technorati,delicious,linkedin,facebook,stumbleupon,digg,google,more", pubid: "ra-4dff56cd6bb1830b" }; Add to shortlist Link Permalink http://dx.doi.org/10.1080/08927022.2011.577074
机译:磷酸二酯酶4D(PDE4D)上调破坏了中枢神经系统中钙离子通道的调节,因此被认为是阿尔茨海默氏病的病因之一。我们采用了基于结构的药物设计技术和全球最大的中药(TCM)数据库来识别潜在的基于TCM的PDE4D抑制剂。然后,我们将多元线性回归(MLR)和支持向量机(SVM)用于定量的构效关系模型以及分子动力学模拟分析。筛选结果表明,金属阳离子Zn 2 + 和Mg 2 + 在介导稳定的蛋白-配体与配体结合残基Asp367和Asp484的相互作用中起关键作用。另外,显示每个配体都干扰暗示抑制作用的活性残基His326。 MLR和SVM预测模型进一步暗示了每种TCM化合物对PDE4D的抑制作用。分子模拟进一步表明每种化合物在PDE4D结合位点的结合稳定性。我们确定了三种中药化合物,例如米糠醛,2-O-阿魏酰基酒石酸和海藻酸,作为潜在的PDE4D抑制剂。此外,我们进一步确定了与蛋白质-配体结合稳定性相关的关键相互作用特征。查看全文下载全文关键词传统中药,对接,支持向量机,分子动力学,阿尔茨海默氏病相关变量var addthis_config = {ui_cobrand:“ Taylor&Francis Online ”,services_compact:“ citeulike,网络振动,微博,technorati,美味,linkedin,facebook,stumbleupon,digg,google,更多”,发布号:“ ra-4dff56cd6bb1830b”};添加到候选列表链接永久链接http://dx.doi.org/10.1080/08927022.2011.577074

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