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A new strategy for full-length Ebola virus glycoprotein expression in ***

A new strategy for full-length Ebola virus glycoprotein expression in ***

作     者:Junjie Zai Yinhua Yi Han Xia Bo Zhang Zhiming Yuan Junjie Zai Yinhua Yi Han Xia Bo Zhang Zhiming Yuan

作者机构:Key Laboratory of Agricultural and Environmental Microbiology Wuhan Institute of Virology Chinese Academy of Sciences Wuhan 430071 China University of Chinese Academy of Sciences Beijing 100049 China Key Laboratory of Special Pathogens and Biosafety Center for Emerging Infectious Diseases WuhanInstitute of Virology Chinese Academy of Sciences Wuhan 430071 China 

出 版 物:《Virologica Sinica》 (中国病毒学(英文版))

年 卷 期:2016年第31卷第6期

页      面:500-508页

核心收录:

学科分类:0710[理学-生物学] 1007[医学-药学(可授医学、理学学位)] 100705[医学-微生物与生化药学] 1002[医学-临床医学] 1001[医学-基础医学(可授医学、理学学位)] 100103[医学-病原生物学] 10[医学] 

基  金:jointly supported by the National Science and Technology Major Project (2012ZX10004219 and 2012ZX10004403) the Presidential Fund of the Chinese Academy of Sciences and the Wuhan Key Laboratory on Emerging Infectious Diseases and Biosafety 

主  题:Ebola virus (EBOV) glycoprotein (GP) E.coli prokaryotic expression 

摘      要:Ebola virus(EBOV) causes severe hemorrhagic fever in humans and non-human primates with high rates of fatality. Glycoprotein(GP) is the only envelope protein of EBOV, which may play a critical role in virus attachment and entry as well as stimulating host protective immune ***, the lack of expression of full-length GP in Escherichia coli hinders the further study of its function in viral pathogenesis. In this study, the vp40 gene was fused to the full-length gp gene and cloned into a prokaryotic expression vector. We showed that the VP40-GP and GP-VP40 fusion proteins could be expressed in *** at 16 ℃. In addition, it was shown that the position of vp40 in the fusion proteins affected the yields of the fusion proteins, with a higher level of production of the fusion protein when vp40 was upstream of gp compared to when it was downstream. The results provide a strategy for the expression of a large quantity of EBOV full-length GP, which is of importance for further analyzing the relationship between the structure and function of GP and developing an antibody for the treatment of EBOV infection.

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