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作 者:郝婷婷[1] 马新廷[1] 朱小飞[1] 卢春[1]
机构地区:[1]南京医科大学微生物与免疫学系,江苏南京210029
出 处:《江苏大学学报(医学版)》2012年第1期14-18,共5页Journal of Jiangsu University:Medicine Edition
基 金:国家自然科学基金资助项目(30972619)
摘 要:目的:构建含有人类免疫缺陷病毒I型(human immunodeficiency virus type Ⅰ,HIV-1)负性调节因子(nega-tive regulation factor,Nef)和增强型绿色荧光蛋白(enhanced green fluorescent protein,EGFP)基因的重组融合蛋白分泌性表达载体,并检测该融合蛋白在真核细胞中的表达及其在培养上清中分泌情况,为进一步研究Nef功能奠定基础。方法:利用PCR扩增出HIV-1 Nef和EGFP基因,插入到分泌性表达载体pSecTag2B中。构建的pSecTag2B-Nef-EGFP融合蛋白表达质粒,转染293T细胞,荧光显微镜下观测细胞中Nef-EGFP融合蛋白的表达。收集细胞及上清液,蛋白质印迹和ELISA法分别检测Nef-EGFP融合蛋白的表达及其分泌。结果:限制性内切酶酶切鉴定和核酸序列测定证实,成功构建了含有Nef-EGFP基因的分泌性表达载体,该质粒转染293T细胞后,蛋白质印迹法能够检测到Nef-EGFP融合蛋白的表达条带,ELISA法检测上清液中目的蛋白分泌量为1.7 ng/ml。结论:成功构建含有Nef-EGFP的融合蛋白表达质粒,融合蛋白Nef-EGFP在293T细胞中获得表达,并能分泌到胞外。Objective: To construct the secretory expression vector containing human immunodeficiency virus type Ⅰ(HIV-1) negative regulation factor(Nef) and enhanced green fluorescent protein(EGFP) gene,and appraise the expression of Nef-EGFP fusion protein in the eukaryotic cell and the secretion into the supernatant.Methods: The Nef and EGFP fragment was amplified by PCR,then cloned into the secretory expression vector pSecTag2B.The recombinant vector pSecTag2B-Nef-EGFP was transfected into the 293T cells,observed the expression of GFP,then harvested the culture media and cells,the fusion protein Nef-EGFP was confirmed by Western blot and ELISA.Results: The recombinant secretory expression vector carried the Nef and EGFP gene was successfully constructed.Western blot analysis revealed that the Nef-EGFP fusion protein can be correctly transcripted and translated in 293T cells,ELISA analysis discovered it can be secreted into the supernatant,the level was 1.7 ng/ml.Conclusion: The recombinant secretory expression vector pSecTag2B-Nef-EGFP was constructed successfully,Nef-EGFP fusion protein could be expressed in 293T cells,and secreted to the supernatant.
关 键 词:分泌性表达载体 人类免疫缺陷病毒Ⅰ型负性调节因子 增强型绿色荧光蛋白 融合蛋白
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