Shen Qingliang, Zeng Danyun, Zhao Baoyu, Bhatt Veer S, Li Pingwei, Cho Jae-Hyun
Department of Biochemistry and Biophysics, Texas A&M University , College Station, Texas 77843, United States.
ACS Chem Biol. 2017 May 19;12(5):1199-1203. doi: 10.1021/acschembio.7b00168. Epub 2017 Apr 5.
The 1918 Spanish influenza A virus (IAV) caused one of the most serious pandemics in history. The nonstructural protein 1 (NS1) of the 1918 IAV hijacks the interaction between human CrkII and JNK1. Little is, however, known about its molecular mechanism. Here, we performed X-ray crystallography, NMR relaxation dispersion experiment, and fluorescence spectroscopy to determine the structural, kinetic, and thermodynamic mechanisms underlying the hijacking of CrkII by 1918 IAV NS1. We observed that the interaction between a proline-rich motif in NS1 and the N-terminal SH3 domain of CrkII displays strikingly rapid kinetics and exceptionally high affinity with 100-fold faster k and 3300-fold lower K compared to those for the CrkII-JNK1 interaction. These results provide molecular insight into the mechanism by which 1918 IAV NS1 hijacks CrkII and disrupts its interactions with critical cellular signaling proteins.
1918年西班牙甲型流感病毒(IAV)引发了历史上最严重的大流行之一。1918年IAV的非结构蛋白1(NS1)劫持了人类CrkII和JNK1之间的相互作用。然而,其分子机制却鲜为人知。在此,我们进行了X射线晶体学、核磁共振弛豫色散实验和荧光光谱分析,以确定1918年IAV NS1劫持CrkII的结构、动力学和热力学机制。我们观察到,NS1中富含脯氨酸的基序与CrkII的N端SH3结构域之间的相互作用表现出惊人的快速动力学和极高的亲和力,与CrkII-JNK1相互作用相比,其结合速率快100倍,解离常数低3300倍。这些结果为1918年IAV NS1劫持CrkII并破坏其与关键细胞信号蛋白相互作用的机制提供了分子层面的见解。