State Key Laboratory of Virology, Wuhan Institute of Virology, Chinese Academy of Sciences, Wuchang District, Wuhan, Hubei, China.
PLoS Pathog. 2013;9(8):e1003549. doi: 10.1371/journal.ppat.1003549. Epub 2013 Aug 8.
The flavivirus NS5 harbors a methyltransferase (MTase) in its N-terminal ≈ 265 residues and an RNA-dependent RNA polymerase (RdRP) within the C-terminal part. One of the major interests and challenges in NS5 is to understand the interplay between RdRP and MTase as a unique natural fusion protein in viral genome replication and cap formation. Here, we report the first crystal structure of the full-length flavivirus NS5 from Japanese encephalitis virus. The structure completes the vision for polymerase motifs F and G, and depicts defined intra-molecular interactions between RdRP and MTase. Key hydrophobic residues in the RdRP-MTase interface are highly conserved in flaviviruses, indicating the biological relevance of the observed conformation. Our work paves the way for further dissection of the inter-regulations of the essential enzymatic activities of NS5 and exploration of possible other conformations of NS5 under different circumstances.
黄病毒 NS5 在其 N 端约 265 个残基中具有一个甲基转移酶(MTase),在 C 端部分具有一个 RNA 依赖性 RNA 聚合酶(RdRP)。NS5 的主要关注点和挑战之一是了解 RdRP 和 MTase 之间的相互作用,因为它是病毒基因组复制和帽形成中独特的天然融合蛋白。在这里,我们报告了来自日本脑炎病毒的全长黄病毒 NS5 的第一个晶体结构。该结构完成了聚合酶基序 F 和 G 的设想,并描绘了 RdRP 和 MTase 之间定义的分子内相互作用。RdRP-MTase 界面中的关键疏水性残基在黄病毒中高度保守,表明观察到的构象具有生物学相关性。我们的工作为进一步剖析 NS5 的必需酶活性的相互调节以及在不同情况下探索 NS5 的可能其他构象铺平了道路。