Xiang Zhufang, Lin Ying, Ye Bo, Han Shuangyan, Zhao Shujin
School of Bioscience and Bioengineering, South China University of Technology, Guangzhou 510006, China.
Sheng Wu Gong Cheng Xue Bao. 2008 Apr;24(4):684-9.
HIV-1 gp41 has been successfully anchored on the cell surface of yeast Saccharomyces cerevisiae by yeast cell-surface display systems using His-tag for the detection of protein expression. Gp41 activity has been detected by gp41 monoclonal antibody. The vector for gp41 yeast display has been constructed as follows: the gene-encoding gp41 was amplified by PCR using pMD18T-gp41 as a template, and then inserted into shuttle vector pICAS-His by restriction enzyme digestion. Next, the vectors were introduced into Saccharomyces cerevisiae MT8-1. After cultivation, recombinant cells were immunofluorescence labelled. The bright green cells were observed by the microscopy indicating the proteins have been displayed on the cell surface successfully, flow cytometry convinced that gp41 has been folded correctly on the cell surface. Then different concentrations of initial glucose were used to enhance the expression of protein. gp41 has been expressed by 82.46% yeast cells as the concentration of glucose was 1%. Protein expression was depressed when the concentration was increased.
通过使用His标签的酵母细胞表面展示系统,HIV-1 gp41已成功锚定在酿酒酵母的细胞表面,用于检测蛋白质表达。已通过gp41单克隆抗体检测到gp41活性。gp41酵母展示载体的构建如下:以pMD18T-gp41为模板,通过PCR扩增编码gp41的基因,然后通过限制性酶切插入穿梭载体pICAS-His。接下来,将载体导入酿酒酵母MT8-1。培养后,对重组细胞进行免疫荧光标记。通过显微镜观察到亮绿色细胞,表明蛋白质已成功展示在细胞表面,流式细胞术证实gp41已在细胞表面正确折叠。然后使用不同浓度的初始葡萄糖来增强蛋白质的表达。当葡萄糖浓度为1%时,82.46%的酵母细胞表达了gp41。当浓度增加时,蛋白质表达受到抑制。