Lee-Huang Sylvia, Huang Philip Lin, Zhang Dawei, Lee Jae Wook, Bao Ju, Sun Yongtao, Chang Young-Tae, Zhang John, Huang Paul Lee
Department of Biochemistry, New York University School of Medicine, New York, NY 10016, USA.
Biochem Biophys Res Commun. 2007 Mar 23;354(4):872-8. doi: 10.1016/j.bbrc.2007.01.071. Epub 2007 Jan 24.
We have identified oleuropein (Ole) and hydroxytyrosol (HT) as a unique class of HIV-1 inhibitors from olive leaf extracts effective against viral fusion and integration. We used molecular docking simulation to study the interactions of Ole and HT with viral targets. We find that Ole and HT bind to the conserved hydrophobic pocket on the surface of the HIV-gp41 fusion domain by hydrogen bonds with Q577 and hydrophobic interactions with I573, G572, and L568 on the gp41 N-terminal heptad repeat peptide N36, interfering with formation of the gp41 fusion-active core. To test and confirm modeling predications, we examined the effect of Ole and HT on HIV-1 fusion complex formation using native polyacrylamide gel electrophoresis and circular dichroism spectroscopy. Ole and HT exhibit dose-dependent inhibition on HIV-1 fusion core formation with EC(50)s of 66-58nM, with no detectable toxicity. Our findings on effects of HIV-1 integrase are reported in the subsequent article.
我们已从橄榄叶提取物中鉴定出橄榄苦苷(Ole)和羟基酪醇(HT),它们是一类独特的HIV-1抑制剂,可有效对抗病毒融合和整合。我们使用分子对接模拟来研究Ole和HT与病毒靶点的相互作用。我们发现,Ole和HT通过与Q577形成氢键以及与gp41 N端七肽重复序列N36上的I573、G572和L568进行疏水相互作用,结合到HIV-gp41融合结构域表面保守的疏水口袋中,从而干扰gp41融合活性核心的形成。为了测试和确认建模预测,我们使用天然聚丙烯酰胺凝胶电泳和圆二色光谱法研究了Ole和HT对HIV-1融合复合物形成的影响。Ole和HT对HIV-1融合核心形成呈现剂量依赖性抑制,半数有效浓度(EC50)为66 - 58 nM,且未检测到毒性。我们关于HIV-1整合酶作用的研究结果将在后续文章中报道。