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作 者:佟敬山[1] 李昌[1] 金宁一[1] 于源华[2] 刘玉生[1] 于芳[1] 胡宁宁[1] 李霄[1] 张钰[1]
机构地区:[1]军事医学科学院十一所病毒室,长春130062 [2]长春理工大学生命科学技术学院,长春130022
出 处:《中国生物制品学杂志》2008年第3期169-173,共5页Chinese Journal of Biologicals
基 金:吉林省应用基础项目(20060570);863计划项目(2006AA02Z447)
摘 要:目的构建二硫键稳定的抗HIV-1 gp41单链抗体(dsFv)基因原核表达载体,并进行表达和鉴定。方法采用PCR定点突变的方法,构建含二硫键稳定的抗HIV-1 gp41单链抗体突变基因质粒pUC57-d41,BamHⅠ和HindⅢ双酶切后,定向插入pET-28a(+),转化大肠杆菌BL21(DE3),IPTG诱导表达,用SDS-PAGE、Western blot鉴定表达产物。对目的蛋白进行纯化和复性,并进行抗原结合活性及相对稳定性检测。结果重组载体pET-d41经酶切鉴定,证实构建正确。表达产物相对分子质量约为28000,与理论预期值完全相符。目的蛋白最高表达量可占菌体总蛋白的45.48%。经Ni-NTA亲和层析法纯化并复性后,蛋白纯度达95%以上,抗HIV-1 gp41 dsFv具有抗原结合活性,稳定性优于scFv。结论已成功构建了二硫键稳定的抗HIV-1 gp41单链抗体(dsFv)基因原核表达载体,并获得表达,为进一步研究其生物学功能奠定了基础。Objective To construct a prokaryotic expression vector for disulfide-stablilized HIV-1 gp41 single chain antibody (dsFv) and identify the expressed product,Methods Amplify disulfide-stabilized HIV-1 gp41 single chain antibody gene by PCR-based point mutagenesis strategy and clone into plasmid pUC57.Digest the constructed recombinant plasmid pUC57-d41 with BamH Ⅰ and Hind Ⅲ and insert the obtained gene fragment into plasmid pET-28a ( + ).Transform the constructed recombinant plasmid pET-d41 to E. coli BL21 (DE3) for expression under induction of IPTG. Identify the expressed product by SDS-PAGE and Western blot. The expressed protein was purified, refolded and determined for antigen binding activity and relative stabihty, Results Restriction analysis proved that recombinant plasmid pET-d41 was correctly constructed. The relative molecular mass of expressed product was about 28 000, which was completely identical to that expected. The expressed prouduct contained 45.48% of total somatic protein and reached a purity of more than 95% after purification by Ni-NTA affinity chromatography. The protein after refolding showed antigen binding activity, and its stability was higher than that of scFv. Conclusion The prokaryotic expression vector for disulfide-stabilized HIV-1 gp41 single chain antibody was successftdly constructed, which laid a foundation of further study on biological function of dsFv.
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