Division of Structural Biology, Centre for Human Genetics, University of Oxford, Oxford, United Kingdom.
Sir William Dunn School of Pathology, University of Oxford, Oxford, United Kingdom.
J Virol. 2024 May 14;98(5):e0013824. doi: 10.1128/jvi.00138-24. Epub 2024 Apr 2.
Influenza A viruses, causing seasonal epidemics and occasional pandemics, rely on interactions with host proteins for their RNA genome transcription and replication. The viral RNA polymerase utilizes host RNA polymerase II (Pol II) and interacts with the serine 5 phosphorylated (pS5) C-terminal domain (CTD) of Pol II to initiate transcription. Our study, using single-particle electron cryomicroscopy (cryo-EM), reveals the structure of the 1918 pandemic influenza A virus polymerase bound to a synthetic pS5 CTD peptide composed of four heptad repeats mimicking the 52 heptad repeat mammalian Pol II CTD. The structure shows that the CTD peptide binds at the C-terminal domain of the PA viral polymerase subunit (PA-C) and reveals a previously unobserved position of the 627 domain of the PB2 subunit near the CTD. We identify crucial residues of the CTD peptide that mediate interactions with positively charged cavities on PA-C, explaining the preference of the viral polymerase for pS5 CTD. Functional analysis of mutants targeting the CTD-binding site within PA-C reveals reduced transcriptional function or defects in replication, highlighting the multifunctional role of PA-C in viral RNA synthesis. Our study provides insights into the structural and functional aspects of the influenza virus polymerase-host Pol II interaction and identifies a target for antiviral development.IMPORTANCEUnderstanding the intricate interactions between influenza A viruses and host proteins is crucial for developing targeted antiviral strategies. This study employs advanced imaging techniques to uncover the structural nuances of the 1918 pandemic influenza A virus polymerase bound to a specific host protein, shedding light on the vital process of viral RNA synthesis. The study identifies key amino acid residues in the influenza polymerase involved in binding host polymerase II (Pol II) and highlights their role in both viral transcription and genome replication. These findings not only deepen our understanding of the influenza virus life cycle but also pinpoint a potential target for antiviral development. By elucidating the structural and functional aspects of the influenza virus polymerase-host Pol II interaction, this research provides a foundation for designing interventions to disrupt viral replication and transcription, offering promising avenues for future antiviral therapies.
甲型流感病毒可引起季节性流行和偶发性大流行,其 RNA 基因组转录和复制依赖于与宿主蛋白的相互作用。病毒 RNA 聚合酶利用宿主 RNA 聚合酶 II(Pol II),并与被丝氨酸 5 磷酸化(pS5)的 C 端结构域(CTD)相互作用,从而启动转录。我们的研究使用单颗粒电子低温显微镜(cryo-EM),揭示了 1918 年大流行的甲型流感病毒聚合酶与合成的 pS5 CTD 肽结合的结构,该肽由四个七肽重复组成,模拟了哺乳动物 Pol II CTD 的 52 个七肽重复。该结构表明,CTD 肽结合在 PA 病毒聚合酶亚基(PA-C)的 C 端结构域,并揭示了 PB2 亚基的 627 结构域在 CTD 附近的一个以前未观察到的位置。我们确定了 CTD 肽中起关键作用的残基,这些残基介导与 PA-C 上带正电荷的腔相互作用,解释了病毒聚合酶对 pS5 CTD 的偏好。针对 PA-C 中 CTD 结合位点的突变体的功能分析表明转录功能降低或复制缺陷,突出了 PA-C 在病毒 RNA 合成中的多功能作用。我们的研究提供了流感病毒聚合酶与宿主 Pol II 相互作用的结构和功能方面的见解,并确定了抗病毒药物开发的靶标。
了解甲型流感病毒与宿主蛋白之间的复杂相互作用对于开发靶向抗病毒策略至关重要。本研究采用先进的成像技术,揭示了与特定宿主蛋白结合的 1918 年大流行甲型流感病毒聚合酶的结构细节,阐明了病毒 RNA 合成的关键过程。该研究确定了流感聚合酶中参与结合宿主 Pol II 的关键氨基酸残基,并强调了它们在病毒转录和基因组复制中的作用。这些发现不仅加深了我们对流感病毒生命周期的理解,还确定了抗病毒药物开发的潜在靶标。通过阐明流感病毒聚合酶与宿主 Pol II 相互作用的结构和功能方面,本研究为设计干预措施以破坏病毒复制和转录提供了基础,为未来的抗病毒治疗提供了有前途的途径。