Department of Immunotherapeutics, Tokyo Medical and Dental University Tokyo, Japan.
Front Microbiol. 2011 Oct 13;2:210. doi: 10.3389/fmicb.2011.00210. eCollection 2011.
Integrase (IN) is a retroviral enzyme that catalyzes the insertion of viral DNA (vDNA) into host chromosomal DNA, which is necessary for efficient viral replication. The crystal structure of prototype foamy virus IN bound to cognate vDNA ends, a complex referred to as the intasome, has recently been resolved. Structure analysis of the intasome revealed a tetramer structure of IN that was required for its catalytic function, and also showed the inhibitory mechanism of the IN inhibitor. Genetic analysis of IN has revealed additional non-enzymatic roles during viral replication cycles at several steps other than integration. However, the higher order structure of IN that is required for its non-enzymatic functions remains to be delineated. This is the next major challenge in the field of IN structural biology hoping to be a platform for the development of novel IN inhibitors to treat human immunodeficiency virus type 1 infectious disease.
整合酶(IN)是一种逆转录病毒酶,能够催化病毒 DNA(vDNA)插入宿主染色体 DNA,这对于有效的病毒复制是必要的。最近已经解析了与同源 vDNA 末端结合的原型泡沫病毒 IN 的晶体结构,该复合物称为整合酶复合物(intasome)。intasome 的结构分析揭示了 IN 的四聚体结构,这是其催化功能所必需的,并且还显示了 IN 抑制剂的抑制机制。对 IN 的遗传分析揭示了在整合以外的几个步骤的病毒复制周期中除了酶活性以外的其他非酶功能。然而,对于其非酶功能所需的 IN 的高级结构仍有待描绘。这是 IN 结构生物学领域的下一个重大挑战,希望它成为开发新型 IN 抑制剂以治疗人类免疫缺陷病毒 1 型传染病的平台。