Structure of Influenza Virus N7: the Last Piece of the Neuraminidase "Jigsaw" Puzzle

被引:35
|
作者
Sun, Xiaoman [1 ,2 ]
Li, Qing [1 ,3 ]
Wu, Yan [1 ]
Wang, Mingyang [1 ]
Liu, Yue [1 ]
Qi, Jianxun [1 ]
Vavricka, Christopher J. [1 ,4 ]
Gao, George F. [1 ,2 ,4 ,5 ]
机构
[1] Chinese Acad Sci, Inst Microbiol, CAS Key Lab Pathogen Microbiol & Immunol, Beijing, Peoples R China
[2] Univ Chinese Acad Sci, Beijing, Peoples R China
[3] Univ Sci & Technol China, Sch Life Sci, Hefei 230026, Anhui, Peoples R China
[4] Chinese Acad Sci, Beijing Inst Life Sci, RNIH, Beijing, Peoples R China
[5] Chinese Ctr Dis Control & Prevent China CDC, Off Director Gen, Beijing, Peoples R China
基金
中国国家自然科学基金;
关键词
A VIRUS; BINDING; ORIGIN; EMERGENCE; OSELTAMIVIR; CALCIUM; SITE;
D O I
10.1128/JVI.00805-14
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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 angstrom and 1.8 angstrom, 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.
引用
收藏
页码:9197 / 9207
页数:11
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