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HBV核心抗原EGFP融合蛋白表达质粒的构建及在Hep G2细胞中的表达
引用本文:徐宁,陈智,姚航平,羊正纲. HBV核心抗原EGFP融合蛋白表达质粒的构建及在Hep G2细胞中的表达[J]. 浙江预防医学, 2005, 17(1): 3-5
作者姓名:徐宁  陈智  姚航平  羊正纲
作者单位:浙江大学医学院附属第一医院传染病研究所、卫生部传染病重点实验室,浙江,杭州,310003
摘    要:
目的探讨采用构建的质粒pHBc-EGFP转染HepG2细胞,瞬时表达HBV核心抗原和增强型绿荧光蛋白的可行性.方法克隆HBV核心抗原基因进入真核表达载体pEGFP-N1中,脂质体法转染HepG2细胞后在荧光显微镜下观察增强型绿荧光蛋白表达,并行RT-PCR及细胞免疫组化分析融合蛋白的表达.结果重组pHBc-EGFP质粒可在HepG2细胞内瞬时表达HBV核心抗原和增强型绿荧光蛋白融合蛋白.结论pHBc-EGFP质粒构建成功,增强型绿荧光蛋白的表达可报告HBV核心抗原表达.

关 键 词:HBV核心抗原  增强型绿荧光蛋白  瞬时表达
文章编号:1007-0931(2005)01-0003-03
修稿时间:2004-07-28

Construction of a Plasmid of HBV Core Antigen-EGFP Fusion Protein and Its Expression in Hep G2 Cell
XU Ning,CHEN Zhi,YAO Hang-ping et al.. Construction of a Plasmid of HBV Core Antigen-EGFP Fusion Protein and Its Expression in Hep G2 Cell[J]. Zhejiang Journal of Preventive Medicine, 2005, 17(1): 3-5
Authors:XU Ning  CHEN Zhi  YAO Hang-ping et al.
Abstract:
Objective To study the transient expression of HBV core antigen and enhanced green fluorescent protein (EGFP) in Hep G 2 cells transfected by a constructed plasmid (pHBc-EGFP). Methods The core antigen gene of HBV was cloned into eukaryotic expression vector pEGFP-N 1, with which Hep G 2 cells were transfected by liposome transfection method. The expression of fusion gene was analyzed by fluorescent microscopy, RT-PCR and immunohistochemistry method, respectively. Results Recombinant plasmid pHBc-EGFP expressed the HBV core antigen-EGFP fusion protein in Hep G 2 cells transiently. Conclusion pHBc-EGFP is constructed successfully, and the expression of EGFP can serve as an indicator reflecting the expression of HBV core antigen gene.
Keywords:HBV core antigen  Enhanced green fluorescent protein  Transient expression
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