National Laboratory of Biomacromolecules, Institute of Biophysics, Chinese Academy of Sciences, Beijing, China.
University of Chinese Academy of Sciences, Beijing, China.
Nat Commun. 2024 May 30;15(1):4607. doi: 10.1038/s41467-024-49047-w.
Type II topoisomerases are ubiquitous enzymes that play a pivotal role in modulating the topological configuration of double-stranded DNA. These topoisomerases are required for DNA metabolism and have been extensively studied in both prokaryotic and eukaryotic organisms. However, our understanding of virus-encoded type II topoisomerases remains limited. One intriguing example is the African swine fever virus, which stands as the sole mammalian-infecting virus encoding a type II topoisomerase. In this work, we use several approaches including cryo-EM, X-ray crystallography, and biochemical assays to investigate the structure and function of the African swine fever virus type II topoisomerase, pP1192R. We determine the structures of pP1192R in different conformational states and confirm its enzymatic activity in vitro. Collectively, our results illustrate the basic mechanisms of viral type II topoisomerases, increasing our understanding of these enzymes and presenting a potential avenue for intervention strategies to mitigate the impact of the African swine fever virus.
II 型拓扑异构酶是普遍存在的酶,在调节双链 DNA 的拓扑构象方面发挥着关键作用。这些拓扑异构酶是 DNA 代谢所必需的,在原核和真核生物中都进行了广泛的研究。然而,我们对病毒编码的 II 型拓扑异构酶的理解仍然有限。一个有趣的例子是非洲猪瘟病毒,它是唯一编码 II 型拓扑异构酶的感染哺乳动物的病毒。在这项工作中,我们使用包括 cryo-EM、X 射线晶体学和生化分析在内的几种方法来研究非洲猪瘟病毒 II 型拓扑异构酶 pP1192R 的结构和功能。我们确定了 pP1192R 在不同构象状态下的结构,并在体外证实了其酶活性。总之,我们的结果阐明了病毒 II 型拓扑异构酶的基本机制,增加了我们对这些酶的理解,并为减轻非洲猪瘟病毒影响的干预策略提供了一个潜在途径。