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作 者:张俊杰[1] 吴元明[1] 刘慧萍[1] 纪宗玲[1] 陈南春[1] 陈苏民[1]
出 处:《细胞与分子免疫学杂志》2001年第1期73-75,共3页Chinese Journal of Cellular and Molecular Immunology
基 金:国家自然科学基金资助!No.39870380;全军医药卫生科研基金资助!No.98M108
摘 要:目的在大肠杆菌中表达人ERA蛋白(h-ERA)和h-ERA C端结构域蛋白,并制备兔抗h-ERA抗血清。方法以 PCR扩增人era基因(h-era)全长cDNA和 h-ERA C端的结构域基因,并分别克隆到(His)6融合表达载体PRSET-C和非融合表达载体pDH中,诱导表达(His)6-h-ERA融合蛋白和h-ERA C端结构域蛋白。用 h-ERA C端结构域蛋白免疫兔,制备兔抗h-ERA抗血清,并以Western-blot对免抗h-ERA抗血清进行鉴定。结果大肠杆菌中表达的h-ERA C端结构域蛋白和(His)6-h-ERA融合蛋白,分别占菌体总蛋白的40%和80%。用兔抗血清可检出大肠杆茵中表达的(His)6-h-ERA融合蛋白。结论 h-ERA和 h-ERA C端结构域蛋白在大肠杆菌中获得高效表达,并成功地制备了兔抗h-ERA抗血清。Aim To express h-ERA and h-ERA C-terminal domain in E. coli and prepare antiserum against human ERA. Methods Human era(h-era) cDNA and h-ERA C-terminal domain gene were amplified by PCR and ligated with prokaryotic expression vector pRSET-C and pDH respectively. E. coli TAP106 transformed with the recombinant plasmid pDH-h-era-C was induced at 42℃ to express h-ERA C-terminal domain protein. Antiserum against h-ERA was prepared by immunizing rabbit with h-ERA C-terminal domain protein purified by SDS-PAGE. E. coli BL21 (DE3) transformed with the recombinant plasmid pRSET-C-h-era was induced with IPTG to express (His)6-h-ERA fusion protein for Western-blot analysis. Results The expressed h-ERA C-terminal domain and (His)6-h-ERA fusion protein occupied about 40% and 80% of total bacterial protein respectively. The(His) 6-h-ERA fusion protein expressed in E. coli can be detected with the rabbit antiserum. Conclusion The h-ERA C-terminal domain protein and (His)6-h-ERA fusion protein were expressed with high efficiency in E. coli, and the rabbit antiserum against h-ERA was prepared successfully.
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