Department of Biomedical Informatics, Asia University, Taichung 41354, Taiwan.
Department of Biomedical Informatics, Asia University, Taichung 41354, Taiwan ; School of Medicine, College of Medicine, China Medical University, Taichung 40402, Taiwan ; Department of Anesthesiology, China Medical University Hospital, Taichung 40447, Taiwan.
Evid Based Complement Alternat Med. 2014;2014:313094. doi: 10.1155/2014/313094. Epub 2014 Apr 30.
The acquired immunodeficiency syndrome (AIDS), caused by the human immunodeficiency virus (HIV), has become a serious world-wide problem because of this disease's rapid propagation and incurability. Recent research has pointed out that the C-C chemokine receptor type 5 (CCR5) is an important target for HIV infection. The traditional Chinese medicine (TCM) database (http://tcm.cmu.edu.tw/) has been screened for molecular compounds that, by simulating molecular docking and molecular dynamics, may protect CCR5 against HIV. Saussureamine C, 5-hydroxy-L-tryptophan, and abrine are selected based on the docking score being higher than Maraviroc and other TCM compounds. The molecular dynamics are helpful in the analysis and detection of protein-ligand interactions. According to the docking poses, hydrophobic interactions, and hydrogen bond variations, this research surmises TRP86, TYR108, GLN194, TYR251, and GLU283 are the main regions of important amino acids in CCR5. In addition to the detection of TCM compound efficacy, we suggest saussureamine C is better than the others for maintaining protein composition during protein-ligand interaction, based on the structural variation.
获得性免疫缺陷综合征(AIDS),由人类免疫缺陷病毒(HIV)引起,由于该疾病的快速传播和不可治愈性,已成为一个严重的世界性问题。最近的研究指出,C-C 趋化因子受体 5(CCR5)是 HIV 感染的一个重要靶点。传统中药(TCM)数据库(http://tcm.cmu.edu.tw/)已被筛选出分子化合物,通过模拟分子对接和分子动力学,可能保护 CCR5 免受 HIV 感染。根据对接评分高于马拉维若和其他 TCM 化合物,选择了钩吻碱 C、5-羟基-L-色氨酸和血根碱。分子动力学有助于分析和检测蛋白质-配体相互作用。根据对接构象、疏水相互作用和氢键变化,本研究推测 CCR5 中重要氨基酸的主要区域是 TRP86、TYR108、GLN194、TYR251 和 GLU283。除了检测 TCM 化合物的疗效外,我们还建议根据结构变化,钩吻碱 C 在维持蛋白质-配体相互作用中的蛋白质组成方面优于其他化合物。