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作 者:逯好英[1,2,3] 金灵[1,2,3] 王宇 王捷[1,2,3] 张晓晖[1,2,3] 尚丹 马贤凯[1,2,3]
机构地区:[1]军事医学科学院基础医学研究所 [2]北京医科大学肝病研究所 [3]广州军区总医院医学实验科
出 处:《军事医学科学院院刊》1998年第2期94-97,共4页Bulletin of the Academy of Military Medical Sciences
基 金:国家"863"高科技资助
摘 要:目的:通过观察影响HCVC基因在大肠杆菌中表达的因素,研制高表达工程菌株,制备重组抗原,用于免疫诊断和生物学功能研究。方法:将2种不同大小的HCVC基因片段克隆到带有PL启动子的表达载体中,通过SDS-PAGE和免疫印迹分析基因表达产物。结果:在观察影响表达因素的基础上,获得了高表达工程菌株,其基因表达产物占菌体蛋白的38.5%。结论:本研究表明。Objective: In order to obtain overexpression product for development of immunodiagnostic assay and study its biological functions, some factors affecting the expression of HCV nucleocapsid gene in E.coli system were observed. Methods: Two gene fragments of the HCV nucleocapsid differing in length were cloned into expression vector with PL promoter. The expressed products were analyzed by SDS PAGE and Western immunoblotting. Results: High level expression was achieved in E.coli system. The expressed product of the gene fragment lacking the hydrophobic carboxyterminus of the HCV nucleocapsid could amount to 38.5% of total bacterial protein in optimum host cells. Conclusion: This study suggests that the gene fragment lacking the hydrophobic carboxyterminus of the HCV nucleocapsid be expressed efficiently in E.coli system.
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