瑶山亚种树鼩ISG15蛋白表达及其多克隆抗体制备  

Expression of ISG15 Protein of Tupaia belangeri yaoshanensis and Preparation of Its Polyclonal Antibody

作　　者：曹颖颖 李慧君 李宝莹 梁亮[1,2] 冷静 唐海波[1,2] CAO Yingying;LI Huijun;LI Baoying;LIANG Liang;LENG Jing;TANG Haibo(Guangxi University of Chinese Medicine,Nanning 530200, China;Guangxi Key Laboratory of Translational Medicine for Treating High-Incidence Infectious Diseases with Integrative Medicine,Nanning 530200,China)

机构地区：[1]广西中医药大学,南宁530200 [2]广西高发传染病中西医结合转化医学重点实验室,南宁530200

出　　处：《中国畜牧兽医》2022年第1期273-282,共10页China Animal Husbandry & Veterinary Medicine

基　　金：国家级大学生创新创业训练计划项目(202010600028);广西自然科学基金项目(2020GXNSFAA297188);广西高校千名中青年骨干教师培育计划(第三期)(桂教师范[2019]81号);广西中医药大学校级重点课题(2020ZD004)。

摘　　要：【目的】克隆瑶山亚种树鼩干扰素刺激基因15(interferon stimulating gene 15,ISG15)基因,在大肠杆菌中高效表达并纯化、制备多克隆抗体,为其生物学应用及检测方法的建立奠定基础。【方法】提取瑶山亚种树鼩外周淋巴细胞总RNA,经RT-PCR扩增出ISG15基因,亚克隆到真核表达载体构建重组真核表达质粒pcDNA3.1-ISG15,并瞬时转染仓鼠肾细胞(baby hamster syrian kidney,BHK-21);同时亚克隆到原核表达载体pET-28a(+)构建重组表达质粒pET-28a-ISG15,转化大肠杆菌BL21(DE3)感受态细胞,IPTG诱导表达树鼩ISG15蛋白;重组蛋白经镍离子亲和层析法纯化并免疫小鼠,获得鼠抗树鼩ISG15多克隆抗体,利用Western blotting和间接免疫荧光技术(IFA)检测其反应性。【结果】成功克隆瑶山亚种树鼩ISG15基因,并构建了其真核和原核表达载体,真核表达载体在BHK-21细胞中能高效表达;原核表达载体在大肠杆菌中30℃、0.5 mmol/L IPTG诱导6 h获得重组蛋白(分子质量22 ku),蛋白以包涵体形式表达,经镍离子亲和层析法得到纯化。乳化后的重组蛋白免疫小鼠,获得抗瑶山亚种树鼩ISG15的多克隆抗体,经Western blotting检测,制备的鼠抗树鼩ISG15多克隆抗体稀释度在1∶8000时仍能够与0.01μg ISG15重组蛋白结合。IFA检测发现,多克隆抗体能与真核细胞过表达的蛋白反应,抗体反应性良好。【结论】构建的原核表达载体在大肠杆菌中高效表达瑶山亚种树鼩ISG15蛋白,重组蛋白纯化复性后具有良好免疫原性,获得的多克隆抗体为进一步研究树鼩抗病毒感染免疫奠定了良好基础。【Objective】The interferon stimulating gene 15(ISG15)gene of Tupaia belangeri yaoshanensis(T.b.yaoshanensis)was cloned,the ISG15 protein was highly expressed and purify in Escherichia coli,then its polyclonal antibody was prepared,which laid the foundation for its biological application and the establishment of detection methods.【Method】Total RNA was extracted from the peripheral lymphocytes of T.b.yaoshanensis,and ISG15 gene was amplified by RT-PCR.ISG15 gene was subcloned into the eukaryotic expression vector to construct the recombinant eukaryotic expression plasmid pcDNA3.1-ISG15,and transiently transfected into renal cells of Cricetidae baby hamster syrian kidney(BHK-21)cells.At the same time,it was subcloned into the prokaryotic expression vector pET-28a(+)and the recombinant expression plasmid pET-28a-ISG15 was constructed.The pET-28a-ISG15 was transformed into E.coli BL21(DE3),and the ISG15 protein of T.b.yaoshanensis was induced by IPTG.The recombinant protein was purified by nickel ion affinity chromatography and immunized with mice to obtain mouse anti-ISG15 polyclonal antibody,and its reactivity was detected by Western blotting and IFA.【Result】ISG15 gene of T.b.yaoshanensis was successfully cloned,and its eukaryotic and prokaryotic expression vectors were constructed.The eukaryotic expression vector could be highly expressed in BHK-21 cells.The prokaryotic expression vector was induced with 0.5 mmol/L IPTG at 30℃for 6 h to obtain the recombinant protein with molecular weight at approximately 22 ku.The protein was expressed in the form of inclusion body and purified by nickel ion affinity chromatography.The mice were immunized with the emulsified recombinant protein to prepare the polyclonal antibody against ISG15 of T.b.yaoshanensis.Western blotting showed that the mouse-anti-T.b.yaoshanensis ISG15 polyclonal antibody could still bind to 0.01μg of ISG15 recombinant protein at the dilution of 1∶8000.IFA tests showed that the antibody could react with the proteins overexpressed by eukary

关 键 词：瑶山亚种树鼩 ISG15 真核表达 原核表达 多克隆抗体 

分 类 号：R392.11[医药卫生—免疫学]