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机构地区:[1]中国医学科学院基础医学研究所,北京协和医学院基础学院,医学分子生物学国家重点实验室,生物化学与分子生物学系,北京100005
出 处:《细胞与分子免疫学杂志》2013年第5期507-510,共4页Chinese Journal of Cellular and Molecular Immunology
基 金:国家科技支撑计划(2012BAI31B08);国家重点实验室专项基金(2060204)
摘 要:目的在大肠杆菌系统表达并纯化人精子肌动蛋白样蛋白7a(ACTL7a)的N段(1-70),制备兔抗ACTL7a多克隆抗体。方法构建重组表达质粒pGEX-6p-1-ACTL7a(1-70),以重组质粒转化E.coli BL21(DE3),筛选阳性重组菌,IPTG诱导目的蛋白表达,通过镍离子金属螯合树脂和谷胱甘肽琼脂糖凝胶4B树脂两次亲和纯化和分子筛分离目的蛋白;以表达的ACTL7a(1-70)蛋白免疫新西兰大白兔,制备抗ACTL7a的多克隆抗体。ELISA检测抗体效价,Western blot法鉴定抗体特异性,免疫荧光组织化学技术检测ACTL7a在曲精小管细胞的表达。结果经IPTG诱导,在大肠杆菌中表达出目的蛋白ACTL7a(1-70),纯化后免疫新西兰大白兔,成功获得抗血清。血清效价达到1:160000以上,且具有良好的特异性。结论成功构建了ACTL7a基因的原核表达载体,并在大肠杆菌中诱导表达,经纯化获得高纯度的目的蛋白;制备出兔抗ACTL7a抗体,效价及特异性均良好。Objective To express and purify the recombinant human sperm actin-like protein 7a (ACTL?a) N terminal (1-70) in E. coli, and prepare the corresponding rabbit anti-ACTLTa polyclonal antibodies. Methods We constructed the recombinant expression plasmid pGEX-6p-I-ACTLTa (1-70), transformed the plasmid into E. coli BL21 (DE3), and selected positive recombinant strain. The target protein was induced to express by IPTG and purified by nickel ions-chelating resin and glutathione sepharose 4B resin, and finally obtained by molecular sieve chromatography. The purified ACTLTa (1-70) protein were used to immunize New Zealand rabbits to prepare anti-ACTLTa polyclonal antibodies. The antibody titers were detected by ELISA, the antibody specificity by Western blotting, and the localization of ACTLTa in the spermatogenic cells of seminifer- ous tubule epithelium by immunofluorescence histochemistry. Results The target protein ACTL?a (1-70) was successfully expressed by IPTG in E. coli, and the corresponding antiserum was obtained in the rabbits immunized with it. The titer of the antiserum reached 1:160 000 and it was proved with a good specificity. Conclusion ACTLTa was expressed in the constructed prokaryotic expression vector. After purification and immunization, high titer and specific anti-ACTL?a antibody was prepared in rabbits.
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