摘要
目的:表达HIV2型基因工程gag抗原。方法:将编码HIV2型gag的部分和全部p55gag1/2基因,克隆到载体pET17b后,分别在E.ColiBL21(DE3)中表达。结果:表达产物为51和61kD融合蛋白,并可与HIV2病人血清发生特异性反应。表达量分别为菌体总蛋白的12.2%和6.2%。结论:上述两种gag重组蛋白可在E.Coli中得到表达,且有良好的抗原性。
Objective: To express HIV2 gag protein in E.coli. Methods: Insert the entire and truncated gag gene into the expressing vector pET17b respectively,then transform and culture E.coli BL21(DE3). Results :Expressed fusion proteins of 51,61 kD could be recognized by serum from HIV2 infected patients. They occupied 12.2% and 6.2% of the expressing host's total proteins respectively. Conclusion: The HIV2 gag recombinant protein could be expressed in E.coli. The expressed gag protein has perfect antigenicity.
出处
《中国免疫学杂志》
CAS
CSCD
北大核心
1999年第6期260-262,共3页
Chinese Journal of Immunology