Comparison of biological activity of recombinant woodchuck interferon gamma and tumor necrosis factor alpha produced in baculovirus and Escherichia coli expression systems

被引:13
|
作者
Wang, J
Michalak, TI
机构
[1] Mem Univ Newfoundland, Fac Med, Ctr Hlth Sci, Div Lab Med, St John, NF A1B 3V6, Canada
[2] Mem Univ Newfoundland, Ctr Hlth Sci, Div Basic Med Sci, St John, NF A1B 3V6, Canada
基金
加拿大创新基金会; 加拿大健康研究院;
关键词
animal model of hepatitis B; antiviral cytokines; cell killing; class I MHC upregulation; woodchuck viral hepatitis;
D O I
10.1016/j.cyto.2004.11.006
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The full-length cDNAs of recombinant woodchuck interferon gamma (rwIFN gamma) and woodchuck tumor necrosis factor alpha (rwTNF alpha) were cloned into baculovirus transfer vectors and expressed in insect Sf9 cells. The recombinant proteins secreted by the insect cells, bac-rwIFN gamma and bac-rwTNF alpha, were found to be functionally competent. Their biological activities were compared to those of rwIFN gamma and rwTNF alpha produced in the Escherichia coli (E. coli) expression system. The bac-rwIFN gamma demonstrated a 4.5-fold greater protective activity against encephalomyocarditis virus-induced cytolysis of woodchuck hepatocytes and that of class I MHC antigen presentation on the hepatocytes than rwIFN gamma derived from E. coli. The bac-rwTNF alpha was cytotoxic towards murine fibroblasts and able to upregulate class I MHC antigen display and these effects were about 18-fold greater than those triggered by rwTNF alpha from E. coli at a comparable protein level. In addition, the antiviral activity of bac-rwIFN gamma was inhibited by anti-wIFN gamma antibodies and the cytotoxicity of bac-rwTNF alpha neutralized by cross-reactive antibodies to murine TNF alpha. The study showed that the expression of rwIFN gamma and rwTNF alpha in the baculovirus system generated biologically active cytokines whose potency was considerably greater than those produced in E. coli. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:22 / 34
页数:13
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