Department of Molecular Physiology and Biological Physics, University of Virginia, Charlottesville, VA, USA.
Nat Rev Microbiol. 2019 Sep;17(9):546-556. doi: 10.1038/s41579-019-0225-2. Epub 2019 Jul 16.
Mammalian cells express a variety of innate immune proteins - known as restriction factors - which defend against invading retroviruses such as HIV-1. Two members of the tripartite motif protein family - TRIM5α and TRIMCyp - were identified in 2004 as restriction factors that recognize and inactivate the capsid shell that surrounds and protects the incoming retroviral core. Research on these TRIM5 proteins has uncovered a novel mode of non-self recognition that protects against cross-species transmission of retroviruses. Our developing understanding of the mechanism of TRIM5 restriction underscores the concept that core uncoating and reverse transcription of the viral genome are coordinated processes rather than discrete steps of the post-entry pathway of retrovirus replication. In this Review, we provide an overview of the current state of knowledge of the molecular mechanism of TRIM5-mediated restriction, highlight recent advances and discuss implications for the development of capsid-targeted antiviral therapeutics.
哺乳动物细胞表达多种先天免疫蛋白——即限制因子——它们可以抵御诸如 HIV-1 等入侵的逆转录病毒。2004 年,三结构域蛋白家族的两个成员——TRIM5α 和 TRIMCyp——被鉴定为限制因子,它们可以识别并失活包裹和保护进入的逆转录病毒核心的衣壳。对这些 TRIM5 蛋白的研究揭示了一种新的非自我识别模式,可以防止逆转录病毒的跨物种传播。我们对 TRIM5 限制机制的理解不断深入,强调了核心脱壳和病毒基因组逆转录是协调的过程,而不是逆转录病毒复制进入后途径的离散步骤。在这篇综述中,我们概述了 TRIM5 介导限制的分子机制的现有知识状态,强调了最近的进展,并讨论了对衣壳靶向抗病毒治疗药物开发的影响。