李震宇 展鹏 刘新泳. HIV-1病毒感染因子Vif及其相关抑制剂的研究进展J. 药学学报, 2010,45(6): 684-693.
引用本文: 李震宇 展鹏 刘新泳. HIV-1病毒感染因子Vif及其相关抑制剂的研究进展J. 药学学报, 2010,45(6): 684-693.
LI Shen-Yu, ZHAN Feng, LIU Xin-Yong. Progress in the study of HIV-1 Vif and related inhibitorsJ. 药学学报, 2010,45(6): 684-693.
Citation: LI Shen-Yu, ZHAN Feng, LIU Xin-Yong. Progress in the study of HIV-1 Vif and related inhibitorsJ. 药学学报, 2010,45(6): 684-693.

HIV-1病毒感染因子Vif及其相关抑制剂的研究进展

Progress in the study of HIV-1 Vif and related inhibitors

  • 摘要:

    HIV-1 (human immunodeficiency virus type 1) 病毒感染因子Vif (viral infectivity factor) 是高度保守的碱性磷酸化蛋白质, HIV-1的辅助调节蛋白之一。Vif蛋白的主要功能是能够介导宿主细胞体内载脂蛋白B mRNA编辑酶催化多肽样蛋白3G (apolipoprotein B mRNA editing enzyme catalytic polypeptide like 3G, APOBEC3G) 的降解, 从而增强病毒的感染性。此外, 它还具有调节病毒的逆转录和复制晚期以及诱导细胞G2期停滞等功能。目前, 许多实验室已经针对Vif蛋白进行抑制剂的设计。本文简要叙述了Vif蛋白的结构与功能, 并主要对其抑制剂的最新进展进行了综述。

     

    Abstract:

    Human immunodeficiency virus type 1 (HIV-1) viral infectivity factor (Vif), one of the accessory proteins, which is a small basic phosphoprotein, is essential for viral replication and pathogenesis.  The best well-characterized function of Vif is its ability to neutralize the host cell antiviral factor, apolipoprotein B  mRNA editing enzyme catalytic polypeptide like 3G (APOBEC3G), which makes the viral particles more infective.  In addition, Vif can regulate the reverse transcription and the advanced stage of replication of the virus particle, as well as induce the termination of cell cycle at G2 stage and so on.  The designed drug aimed directly at    Vif can efficiently block the maturation and infectivity of HIV-1.  In this review, the structure, function and   especially the related inhibitors of Vif are reviewed.

     

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