GST-HPV16E7融合蛋白的原核表达与纯化  

Expression and Purification of GST-HPV16E7 Fusion Protein

作　　者：张健[1] 王涛[2] 郄明蓉[1] 韩敏[1] 陈悦[1] 

机构地区：[1]四川大学华西第二医院妇产科,成都610041 [2]四川大学华西第二医院分子与转化实验室,成都610041

出　　处：《四川大学学报（医学版）》2009年第6期1123-1126,共4页Journal of Sichuan University(Medical Sciences)

摘　　要：目的构建HPV16地方株E7基因原核表达质粒,使其在原核细胞中高效表达并进行纯化。方法将成都本地某宫颈癌患者所感染的HPV16E7全长片段插入原核表达载体pGEX-4T-1,构建重组子pGEX-4T-1-HPV16E7,转化宿主菌E.coliBL-21。经IPTG诱导表达,通过SDS-PAGE、Western blot分析证实蛋白表达的特异性。并用GST亲和层析法对融合蛋白进行纯化。结果该患者所感染的HPV16为东亚株,成功构建了原核表达载体pGEX-4T-1-HPV16E7并表达出GST-HPV16E7融合蛋白,证实了蛋白表达的特异性,并获得了GST-HPV16E7融合蛋白的纯品。结论成功表达、纯化了本地流行株GST-HPV16E7融合蛋白,为进一步研究HPV16E7蛋白的功能奠定了实验基础。Objective To construct a recombinant prokaryotic expression vector efficiently expressing HPV16 E7 and purify GST-HPV16E7 fusion protein.Methods The HPV16 E7 gene obtained from a local cervical cancer patient was cloned into vector pGEX-4T-1,to generate the recombinant named as pGEX-4T-1-HPV16 E7.The recombinant plasmid was transformed into E.coli BL21.After inducing with IPTG the HPV16E7 fusion protein was analyzed by SDS-PAGE and Western blot.B-PER GST Fusion Protein Purification Kit was appkied to purify GST-HPV16E7 fusion protein.Results The recombinant plasmid pGEX-4T-1-HPV16 E7 was successfully constructed.Highly expressed and purified GST-HPV16E7 fusion protein was obtained.The specificity of fusion protein was verified by SDS-PAGE and Western blot.Conclusion GST-HPV16E7 fusion protein was successfully expressed and purified.

关 键 词：人乳头瘤病毒 E7 东亚株 原核表达 宫颈癌 

分 类 号：R737.33[医药卫生—肿瘤]