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通过虚拟筛选和生物评估鉴定靶向 HIV-1 Vif 和人 APOBEC3G 相互作用的小分子化合物。

Identification of small molecule compounds targeting the interaction of HIV-1 Vif and human APOBEC3G by virtual screening and biological evaluation.

机构信息

Institute of Medicinal Biotechnology, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China.

Lady Davis Institute for Medical Research, Jewish General Hospital, McGill University, Montreal, QC, Canada.

出版信息

Sci Rep. 2018 May 23;8(1):8067. doi: 10.1038/s41598-018-26318-3.

Abstract

Human APOBEC3G (hA3G) is a restriction factor that inhibits human immunodeficiency 1 virus (HIV-1) replication. The virally encoded protein Vif binds to hA3G and induces its degradation, thereby counteracting the antiviral activity of hA3G. Vif-mediated hA3G degradation clearly represents a potential target for anti-HIV drug development. Herein, we have performed virtual screening to discover small molecule inhibitors that target the binding interface of the Vif/hA3G complex. Subsequent biochemical studies have led to the identification of a small molecule inhibitor, IMB-301 that binds to hA3G, interrupts the hA3G-Vif interaction and inhibits Vif-mediated degradation of hA3G. As a result, IMB-301 strongly inhibits HIV-1 replication in a hA3G-dependent manner. Our study further demonstrates the feasibility of inhibiting HIV replication by abrogating the Vif-hA3G interaction with small molecules.

摘要

人载脂蛋白 B mRNA 编辑酶催化多肽 3G(hA3G)是一种限制因子,可抑制人类免疫缺陷病毒 1 型(HIV-1)的复制。病毒编码的蛋白 Vif 与 hA3G 结合并诱导其降解,从而抵消 hA3G 的抗病毒活性。Vif 介导的 hA3G 降解显然代表了抗 HIV 药物开发的潜在靶点。在此,我们进行了虚拟筛选,以发现靶向 Vif/hA3G 复合物结合界面的小分子抑制剂。随后的生化研究鉴定出一种小分子抑制剂 IMB-301,它与 hA3G 结合,阻断 hA3G-Vif 相互作用并抑制 Vif 介导的 hA3G 降解。因此,IMB-301 强烈抑制 HIV-1 复制,这依赖于 hA3G。我们的研究进一步证明了用小分子阻断 Vif-hA3G 相互作用抑制 HIV 复制的可行性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4891/5966509/bc00941d68b0/41598_2018_26318_Fig1_HTML.jpg

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