周良,陈杰,唐双阳,李薇,余敏君,朱翠明,万艳平.人乳头瘤病毒16型E2蛋白真核载体的构建与表达.[J].中南医学科学杂志.,2011,39(1):55-57.
人乳头瘤病毒16型E2蛋白真核载体的构建与表达
Expression and Construction of Eukaryotic Vector of HPV16 E2 Protein
投稿时间:2010-06-11  
DOI:
中文关键词:  人乳头瘤病毒16型  E2  表达
英文关键词:HPV16  E2  expression
基金项目:湖南省科学技术厅计划项目(2009FJ3048).
作者单位
周良1,2,陈杰1,唐双阳1,李薇1,余敏君1,朱翠明1,万艳平1 1.南华大学 病原生物学研究所湖南 衡阳4210012.怀化医学高等专科学校 
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中文摘要:
      目的构建人乳头瘤病毒16型(HPV16)E2蛋白真核载体,为研究其基因疫苗免疫活性奠定实验基础。方法PCR扩增HPV16 E2基因片段,将其连接到真核表达载体pcDNA3.1(+),双酶切及测序鉴定。将质粒pcDNA3.1(+)与pcDNA3.1(+)/HPV16 E2分别转染HeLa细胞,RT-PCR鉴定E2基因在HeLa细胞中的表达。结果HPV16 E2基因片段插入到pcDNA3.1(+)相同酶切位点,即构建了真核表达载体pcDNA3.1(+)/HPV16 E2;转染pcDNA3.1(+)/HPV16 E2的细胞,检测到HPV16 E2 mRNA。结论构建的真核表达载体pcDNA3.1(+)/HPV16 E2能在HeLa细胞内有效表达。
英文摘要:
      ObjectiveTo provide the experimental basis for further researching immunological competence of human papillomavirus type 16 (HPV16) E2 gene vaccine,eukaryotic expression vector of HPV16 E2 protein is constructed.MethodsHPV16 E2 gene fragment amplified by PCR was inserted into eukaryotic expression vector of pcDNA3.1(+) with the same restriction sites.Enzymes digestion and DNA sequencing were used to identify E2 gene fragment.The eukaryotic expression vector of pcDNA3.1(+) or pcDNA3.1(+)/HPV16 E2 was transfected into HeLa cells,respectively.The expression of HPV16 E2 was analyzed using RT-PCR.ResultsThe gene fragment of HPV16 E2 was successfully insert into pcDNA3.1(+).The mRNA products of HPV16 E2 were detected in the cells transfected with pcDNA3.1(+)/HPV16 E2.ConclusionEukaryotic expression vector of pcDNA3.1(+)/HPV16 E2 successfully express HPV16 E2 mRNA in HeLa cells.
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