Wang Ziyu, Zhang Jianqiong
Bing Du Xue Bao. 2016 Sep;32(5):634-9.
The human immunodeficiency virus type 1(HIV-1)has spread globally and often exhibits antiviral resistance. Therefore, there is an ongoing need for the development of novel, highly efficient antiretroviral drugs with low toxicity. The capsid protein(CA),which is composed of an N-terminal domain(NTD)and C-terminal domain(CTD),plays an important role in the process of HIV-1assembly and maturation. In recent years, the structure of capsid protein has been solved. In this article, we summarizes the spatial structure of the HIV-1capsid protein determined by X-ray crystallography, and describe the structural characteristics of the NTD-NTD,NTD-CTD and CTD-CTD interfaces. This article summarizes the antiviral approaches targeting CA and expounds a new strategy in combination with CRISPR/Cas9 gene editing technology.
1型人类免疫缺陷病毒(HIV-1)已在全球传播,且常表现出抗病毒耐药性。因此,持续需要开发新型、高效且低毒的抗逆转录病毒药物。由N端结构域(NTD)和C端结构域(CTD)组成的衣壳蛋白(CA)在HIV-1组装和成熟过程中发挥着重要作用。近年来,衣壳蛋白的结构已得到解析。在本文中,我们总结了通过X射线晶体学确定的HIV-1衣壳蛋白的空间结构,并描述了NTD-NTD、NTD-CTD和CTD-CTD界面的结构特征。本文总结了针对CA的抗病毒方法,并阐述了结合CRISPR/Cas9基因编辑技术的新策略。