LI Yue-Xi, TANG Jia-Qi, SHI Jiang, ZHAO Hua-Zhong and JIAO Ren-Liang. Expression of HCV Core Protein in E.c0fi and Its Application[J]. Virologica Sinica, 1994, 9(1).
Citation: LI Yue-Xi, TANG Jia-Qi, SHI Jiang, ZHAO Hua-Zhong, JIAO Ren-Liang. Expression of HCV Core Protein in E.c0fi and Its Application .VIROLOGICA SINICA, 1994, 9(1) : 18.

丙型肝炎病毒核心蛋白基因在大肠杆菌内的表达及应用

  • 将从中国丙肝病人血清中扩增克隆的丙型肝炎病毒核心蛋白基因(408bp)酶切处理后插入表达载体pJLA502内,获得高表达核心蛋白的重组工程菌。将重组菌经42℃热诱导5h,SDS-PAGE分析表明,表达的核心蛋白占菌体蛋白总量的20%。经分子筛和吸附层析纯化后获得的核心蛋白,ELISA检测证实有较好的抗原性和特异性。用表达的核心抗原加用表达的NS_3抗原(C_33)装配的抗-HCV试剂盒,经用标准血清验证及与国外第二代抗-HCV试剂盒比较,证实符合丙肝诊断试剂要求。

Expression of HCV Core Protein in E.c0fi and Its Application

  • The cloned HCV core protein gene was inserted into the plasmid vector pJLA502 at EcoRI site,and the recombinant plasmid was transformed into E,coli DH_(5a),After inducing 5hrs at 42℃,SDS-PAGE analysis showed that the expressed core protein is twenty percent of total protein of E.coliDH5a;the purified core protein by Sephadex G200 gel filtration and Sepharose-4B-IgG affinity chro-matography has excellent antigenicity and specificity,and is good for detecting anti-HCV.

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    Expression of HCV Core Protein in E.c0fi and Its Application

    • 1. Nanjing Military Medical Research Institute,Nanjing 210002

    Abstract: The cloned HCV core protein gene was inserted into the plasmid vector pJLA502 at EcoRI site,and the recombinant plasmid was transformed into E,coli DH_(5a),After inducing 5hrs at 42℃,SDS-PAGE analysis showed that the expressed core protein is twenty percent of total protein of E.coliDH5a;the purified core protein by Sephadex G200 gel filtration and Sepharose-4B-IgG affinity chro-matography has excellent antigenicity and specificity,and is good for detecting anti-HCV.

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