整合酶
模仿
整合酶抑制剂
功能(生物学)
分子模拟
tar(计算)
核糖核酸
病毒学
生物
计算生物学
人类免疫缺陷病毒(HIV)
遗传学
基因
抗逆转录病毒疗法
动物
免疫系统
计算机科学
病毒载量
程序设计语言
作者
Ganjam V. Kalpana,Emilie Ernst,Swati Haldar
出处
期刊:Viruses
[Multidisciplinary Digital Publishing Institute]
日期:2025-05-11
卷期号:17 (5): 693-693
被引量:1
摘要
HIV-1 integrase (IN), an essential viral protein that catalyzes integration, also influences non-integration functions such as particle production and morphogenesis. The mechanism by which non-integration functions are mediated is not completely understood. Several factors influence these non-integration functions, including the ability of IN to bind to viral RNA. INI1 is an integrase-binding host factor that influences HIV-1 replication at multiple stages, including particle production and particle morphogenesis. IN mutants defective for binding to INI1 are also defective for particle morphogenesis, similar to RNA-binding-defective IN mutants. Studies have indicated that the highly conserved Repeat (Rpt) 1, the IN-binding domain of INI1, structurally mimics TAR RNA, and that Rpt1 and TAR RNA compete for binding to IN. Based on the RNA mimicry, we propose that INI1 may function as a “place-holder” for viral RNA to facilitate proper ribonucleoprotein complex formation required during the assembly and particle morphogenesis of the HIV-1 virus. These studies suggest that drugs that target IN/INI1 interaction may lead to dual inhibition of both IN/INI1 and IN/RNA interactions to curb HIV-1 replication.
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