Department of Biochemistry and Biophysics, Texas A&M University, College Station, TX 77843, USA.
Viruses. 2020 Mar 20;12(3):338. doi: 10.3390/v12030338.
The 1918 influenza A virus (IAV) caused the worst flu pandemic in human history. Non-structural protein 1 (NS1) is an important virulence factor of the 1918 IAV and antagonizes host antiviral immune responses. NS1 increases virulence by activating phosphoinositide 3-kinase (PI3K) via binding to the p85β subunit of PI3K. Intriguingly, unlike the NS1 of other human IAV strains, 1918 NS1 hijacks another host protein, CRK, to form a ternary complex with p85β, resulting in hyperactivation of PI3K. However, the molecular basis of the ternary interaction between 1918 NS1, CRK, and PI3K remains elusive. Here, we report the structural and thermodynamic bases of the ternary interaction. We find that the C-terminal tail (CTT) of 1918 NS1 remains highly flexible in the complex with p85β. Thus, the CTT of 1918 NS1 in the complex with PI3K can efficiently hijack CRK. Notably, our study indicates that 1918 NS1 enhances its affinity to p85β in the presence of CRK, which might result in enhanced activation of PI3K. Our results provide structural insight into how 1918 NS1 hijacks two host proteins simultaneously.
1918 年甲型流感病毒(IAV)引发了人类历史上最严重的流感大流行。非结构蛋白 1(NS1)是 1918 年 IAV 的一个重要毒力因子,它拮抗宿主抗病毒免疫反应。NS1 通过与 PI3K 的 p85β 亚基结合激活磷酯酰肌醇 3-激酶(PI3K)从而增加病毒的毒力。有趣的是,与其他人类 IAV 株的 NS1 不同,1918 年 NS1 劫持另一种宿主蛋白 CRK 与 p85β 形成三元复合物,导致 PI3K 的过度激活。然而,1918 年 NS1、CRK 和 PI3K 之间三元相互作用的分子基础仍不清楚。在这里,我们报告了三元相互作用的结构和热力学基础。我们发现,1918 NS1 的 C 端尾部(CTT)在与 p85β 的复合物中保持高度灵活。因此,1918 NS1 在与 PI3K 的复合物中的 CTT 可以有效地劫持 CRK。值得注意的是,我们的研究表明,1918 NS1 在 CRK 存在的情况下增强了其与 p85β 的亲和力,这可能导致 PI3K 的激活增强。我们的研究结果为 1918 NS1 如何同时劫持两种宿主蛋白提供了结构上的见解。