摘要
目的高效表达TAT—HBX—EGFP融合蛋白,研究其在小鼠肝脏内的分布。方法构建TAT-HBX—EGFP重组载体,IPTG诱导使其在BL21中大量表达;蛋白经Ni柱纯化后注射入小鼠体内,免疫荧光观察TAT,HBX—EGFP融合蛋白在小鼠肝脏的分布。结果TAT,HBX—EGFP在大肠埃希菌中获得高效表达;HBX蛋白可以在TAT的引导下进入小鼠肝脏。结论TAT引导肽可以将HBX蛋白引导至小鼠肝脏。
Objective To highly express TAT-HBX-EGFP fusion protein and study its distribution in mouse liver. Methods TAT-HBX-EGFP recombinant vector was constructed and fusion protein was induced by IPTG and expression in BI221 ; fusion protein was purified by Ni-NTA argarose, then injected into the peritoneal cavity of the mice. Distribution of fusion protein was observed by immunofluoreseence. Results TAT-HBX-EGFP was highly expression in E. coli; HBX could be induced into mouse liver by TAT. Conclusion HBX protein could be induced into mouse liver by TAT induced peptide.
出处
《中华实验和临床病毒学杂志》
CAS
CSCD
北大核心
2008年第4期287-289,共3页
Chinese Journal of Experimental and Clinical Virology
基金
北京市丰台区科委科技项目(xm070086)