Retroviral integrase: Structure, mechanism, and inhibition.

Q3 Biochemistry, Genetics and Molecular Biology
Enzymes Pub Date : 2021-01-01 Epub Date: 2021-08-23 DOI:10.1016/bs.enz.2021.06.007
Dario Oliveira Passos, Min Li, Robert Craigie, Dmitry Lyumkis
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引用次数: 5

Abstract

The retroviral protein Integrase (IN) catalyzes concerted integration of viral DNA into host chromatin to establish a permanent infection in the target cell. We learned a great deal about the mechanism of catalytic integration through structure/function studies over the previous four decades of IN research. As one of three essential retroviral enzymes, IN has also been targeted by antiretroviral drugs to treat HIV-infected individuals. Inhibitors blocking the catalytic integration reaction are now state-of-the-art drugs within the antiretroviral therapy toolkit. HIV-1 IN also performs intriguing non-catalytic functions that are relevant to the late stages of the viral replication cycle, yet this aspect remains poorly understood. There are also novel allosteric inhibitors targeting non-enzymatic functions of IN that induce a block in the late stages of the viral replication cycle. In this chapter, we will discuss the function, structure, and inhibition of retroviral IN proteins, highlighting remaining challenges and outstanding questions.

逆转录病毒整合酶:结构、机制和抑制。
逆转录病毒蛋白整合酶(IN)催化病毒DNA与宿主染色质协调整合,从而在靶细胞中建立永久性感染。在过去四十年的IN研究中,我们通过结构/功能研究了解了大量关于催化整合机制的信息。作为三种必需的逆转录酶之一,IN也成为抗逆转录病毒药物治疗艾滋病毒感染者的目标。阻断催化整合反应的抑制剂现在是抗逆转录病毒治疗工具包中最先进的药物。HIV-1 IN还具有与病毒复制周期后期相关的有趣的非催化功能,但这方面的了解仍然很少。也有针对IN的非酶功能的新型变构抑制剂,在病毒复制周期的后期诱导阻断。在本章中,我们将讨论逆转录病毒In蛋白的功能、结构和抑制作用,强调仍然存在的挑战和悬而未决的问题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Enzymes
Enzymes Biochemistry, Genetics and Molecular Biology-Biotechnology
CiteScore
4.30
自引率
0.00%
发文量
10
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