CAS Key Laboratory of Pathogenic Microbiology and Immunology, Institute of Microbiology, Chinese Academy of Sciences, Beijing, China University of Chinese Academy of Sciences, Beijing, China.
CAS Key Laboratory of Pathogenic Microbiology and Immunology, Institute of Microbiology, Chinese Academy of Sciences, Beijing, China School of Life Sciences, University of Science and Technology of China, Hefei, Anhui Province, China.
J Virol. 2014 Aug;88(16):9197-207. doi: 10.1128/JVI.00805-14. Epub 2014 Jun 4.
There are nine subtypes of influenza A virus neuraminidase (NA), N1 to N9. In addition, influenza B virus also contains NA, and there are two influenza virus NA-like molecules, N10 and N11, which were recently identified from bats. Crystal structures for all of these proteins have been solved, with the exception of N7, and there is no published report of N6, although a structure has been deposited in the Protein Data Bank. Here, we present the N7 and N6 structures at 2.1 Å and 1.8 Å, respectively. Structural comparison of all NA subtypes shows that both N7 and N6 highly resemble typical group 2 NA structures with some special characteristics, including an additional cavity adjacent to their active sites formed by novel 340-loop conformations. Comparative analysis also revealed new structural insights into the N-glycosylation, calcium binding, and second sialic acid binding site of influenza virus NA. This comprehensive study is critical for understanding the complexity of the most successful influenza drug target and for the structure-based design of novel influenza inhibitors.
Influenza viruses impose a great burden on society, by the human-adapted seasonal types as well as by variants that occasionally jump from the avian reservoir to infect humans. The surface glycoprotein neuraminidase (NA) is essential for the propagation of the virus and currently the most successfully drug-targeted molecule. Therefore, the structural and functional analysis of NA is critical for the prevention and control of influenza infections. There are nine subtypes of influenza A virus NA (N1 to N9). In addition, influenza B virus also contains NA, and there are two influenza NA-like molecules, N10 and N11, which were recently identified in bats. Crystal structures for all of these proteins have been solved and reported with the exception of N7 and N6. The structural analysis of influenza virus N7 and N6 presented in this study therefore completes the puzzle and adds to a comprehensive understanding of influenza virus NA.
流感病毒 A 有 9 种神经氨酸酶(NA)亚型,分别为 N1 至 N9。此外,流感 B 病毒也含有 NA,还有两种类似流感病毒 NA 的分子,N10 和 N11,它们最近在蝙蝠中被发现。除了 N7 之外,所有这些蛋白质的晶体结构都已经被解决,并且没有关于 N6 的发表报告,尽管有一个结构已经被存入蛋白质数据库。在这里,我们分别以 2.1 Å 和 1.8 Å 的分辨率呈现 N7 和 N6 的结构。对所有 NA 亚型的结构比较表明,N7 和 N6 与典型的第 2 组 NA 结构高度相似,具有一些特殊的特征,包括其活性部位附近由新型 340 环构象形成的额外空腔。比较分析还揭示了流感病毒 NA 的 N-糖基化、钙结合和第二个唾液酸结合位点的新结构见解。这项全面的研究对于理解最成功的流感药物靶点的复杂性以及新型流感抑制剂的结构基础设计至关重要。
流感病毒对社会造成了巨大的负担,既包括适应人类的季节性类型,也包括偶尔从禽类宿主跳跃感染人类的变异体。表面糖蛋白神经氨酸酶(NA)是病毒繁殖所必需的,目前是最成功的靶向药物分子。因此,NA 的结构和功能分析对于流感感染的预防和控制至关重要。流感病毒 A 有 9 种神经氨酸酶(NA)亚型(N1 至 N9)。此外,流感 B 病毒也含有 NA,还有两种类似流感病毒 NA 的分子,N10 和 N11,它们最近在蝙蝠中被发现。除了 N7 和 N6 之外,所有这些蛋白质的晶体结构都已经被解决并报告。因此,本研究中对流感病毒 N7 和 N6 的结构分析完成了拼图,增加了对流感病毒 NA 的全面理解。