吉林大学学报(理学版) ›› 2019, Vol. 57 ›› Issue (06): 1538-1543.

• 生物科学 • 上一篇    下一篇

重组人源抗血管内皮生长因子单克隆抗体的制备及鉴定

董雪1, 徐雨昕2, 郭晶1, 龚忠阔1, 夏霖亚1, 殷玉和1, 吴丛梅1   

  1. 1. 长春工业大学 化学与生命科学学院, 长春 130012; 
    2. 东北农业大学 生命科学学院, 哈尔滨 150030
  • 收稿日期:2018-12-13 出版日期:2019-11-26 发布日期:2019-11-21
  • 通讯作者: 吴丛梅 E-mail:wucmyue@sina.com

Preparation and Identification of Recombinant-Humanized AntiVEGF Monoclonal Antibody

DONG Xue1, XU Yuxin2, GUO Jing1, GONG Zhongkuo1,XIA Linya1, YIN Yuhe1, WU Congmei1   

  1. 1. School of Chemistry and Life Science, Changchun University of Technology, Changchun 130012, China;2. College of Life Science, Northeast Agricultural University, Harbin 150030, China
  • Received:2018-12-13 Online:2019-11-26 Published:2019-11-21
  • Contact: WU Congmei E-mail:wucmyue@sina.com

摘要: 通过优化密码子获得带有信号肽的人源抗血管内皮生长因子(VEGF)抗体的重链和轻链DNA序列, 分别构建表达载体pcDNAVEGFH和pcDNAVEGFV, 将表达载体共转染HEK293细胞后, 与C6胶质瘤细胞共培养, 并将所得蛋白进行分离纯化. 实验结果表明: pcDNAVEGFH和pcDNAVEGFV共转染HEK293F细胞, 可显著抑制C6细胞增殖(P<0.01); 转染24~144 h后的细胞培养上清液中均有蛋白表达; 所得纯化蛋白和标准品一致; 纯化所得抗体蛋白能明显抑制C6细胞增殖(P<005~001), 与标准品抑制效果相似.

关键词: 密码子优化, VEGF单克隆抗体, 纯化, 生物活性

Abstract: DNA sequences of humanized antiVEGF antibody light and heavy chains were optimized to construct pcDNAVEGFH and pcDNAVEGFV expression vectors with signal peptidetide. HEK293 cells were transfected with pcDNAVEGFH and pcDNAVEGFV, then cocultured with C6 cells, and protein was isolated and purified. The experimental results show that the proliferation of C6 cells are significantly inhibited (P<0.01). HEK293F cells are transfected with pcDNAVEGFH and pcDNAVEGFV, expression of protein is detected in cell culture supernate after 24~144 h. The purified protein is identical with the standard product. The purified antibody protein can significantly inhibit the proliferation of C6 cells (P<0.05—0.01). The results are similar to those of standard products.

Key words: codon optimization, antiVEGF monoclonal antibody, purification, biological activity

中图分类号: 

  • Q78