Tat融合蛋白表达载体TAT-SOX2的克隆化及蛋白表达研究

摘要

目的 构建重组表达载体TAT-SOX2,在E.coli BL21中高效表达并纯化融合蛋白.方法 经PCR获得编码人SOX2的全基因序列,连接到原核表达载体PET-28b-TAT-V2上,得到重组表达载体TAT-SOX2,转化大肠埃希菌,IPTG诱导TAT-SOX2融合蛋白的表达.表达产物用SDS-PAGE鉴定,亲和层析柱纯化融合蛋白,并应用Western Blot检测蛋白的特异性,应用免疫荧光检测融合蛋白转导HSF细胞的效果.结果 成功构建了TAT-SOX2融合蛋白的原核表达载体,在诱导下获得了高效表达并纯化了融合蛋白,Western Blot鉴定正确.免疫荧光提示融合蛋白可快速转导入HSF细胞内.结论 为进一步的通过蛋白转导方式诱导多能干细胞提供了物质基础.%Objective To construct recombinant expression vector TAT-SOX2 and express the fusion protein in E.coli BL21.Methods SOX2 fragment were amplified by PCR.The product was digested with restriction enzymes then was inserted into PET-28b-TAT-V2 which contains protein transduction domain of TAT.The recombinant vector was transformed into E.coli BL and induced with IPTG.The expressed fusion protein was analyzed by using SDS-PAGE method.The highly expressed product was purified by affinity chromatography.Western blotting was used to identify the specificity of the fusion protein.The immunofluorescence was used to detect the efficiency of fusion protein transduced to HSF cells.Results The recombinant expression vector TAT-SOX2 was correctly constructed and fusion protein TAT-SOX2 was successfully expressed in prokaryotic cells.Western blotting showed the specificity of the fusion protein.The immunofluorescence prompt fusion protein was transduced into HSF cells quickly.Conclusion This study provides the material basis for the further induced pluripotent stem cells by protein transduction.