HEV保护性基因工程抗体的制备及功能研究
作者:
作者单位:

作者简介:

通讯作者:

中图分类号:

基金项目:

中国博士后科学基金(1851);南京市医学科技发展项目(ZKX15051)


Preparation and function study of the protective HEV genetically engineered antibody
Author:
Affiliation:

Fund Project:

  • 摘要
  • |
  • 图/表
  • |
  • 访问统计
  • |
  • 参考文献
  • |
  • 相似文献
  • |
  • 引证文献
  • |
  • 资源附件
  • |
  • 文章评论
    摘要:

    目的:制备抗戊型肝炎病毒(hepatitis E virus,HEV)的人鼠嵌合基因工程抗体并研究其中和保护作用及特性。方法:将已获得的抗HEV鼠源单克隆抗体基因序列进行优化,设计人鼠嵌合的工程化抗体基因序列,将其克隆入真核表达载体;表达载体共转染293F细胞进行表达优化,高效制备基因工程化抗体;通过酶联免疫反应(enzyme linked immunosorbent assay,ELISA)、免疫荧光及HEV细胞感染模型,研究工程化抗体的结合能力及中和活性。结果:成功构建基因工程化人鼠嵌合HEV保护性抗体表达载体,在293F表达系统中实现高效表达。抗体表达产率达30 mg/L,亲和力为1.202×10-8 mol/L。免疫荧光检测结果显示抗体能够灵敏、特异地与已感染HEV的 Kernow细胞结合,实时荧光定量PCR检测结果显示抗体可保护易感的C3A细胞不被HEV感染。结论:基因工程化抗体抗体具有高效的HEV结合能力及中和作用,能有效阻断HEV感染,并实现低成本高效表达。

    Abstract:

    Objective:This study amis to prepare the genetically engineered human-mouse chimeric antibody against hepatitis E virus(HEV)and investigate its protective neutralization and properties. Methods:To optimize the obtained anti-HEV murine monoclonal antibody gene sequence,the human-mouse chimeric engineered antibody gene sequences were designed and cloned into the antibody eukaryotic expression vectors;vectors were co-transfected into 293F cells for optimal expression,and the genetically engineered antibody was efficiently prepared. The binding ability and neutralizing activity of the engineered antibody was studied by enzyme linked immunosorbent assay(ELISA),immunofluorescence and HEV cell infection model. Results:The engineered human-mouse chimeric HEV protective antibody expression vectors were constructed successfully,and the engineered human-mouse chimeric HEV protective antibody was expressed in the 293F expression system efficiently. Antibody expression yield reached 30 mg/L,binding affinity of the antibody was 1.202×10-8 mol/L. Immunofluorescence results showed that the antibody could sensitively and specifically bind to Kernow cells infected by HEV. The results of quantitative real-time PCR showed that the antibody could protect susceptible C3A cells from HEV infection. Conclusion:Gene engineering antibody has high HEV binding capacity and efficient neutralization protection,which can effectively block HEV infection and be achieved with low-cost and high-efficiency.

    参考文献
    相似文献
    引证文献
引用本文

李 冰,杨婷婷,唐 奇,冯振卿,杨永林,陈 宇. HEV保护性基因工程抗体的制备及功能研究[J].南京医科大学学报(自然科学版),2020,(3):342-347

复制
分享
文章指标
  • 点击次数:
  • 下载次数:
  • HTML阅读次数:
  • 引用次数:
历史
  • 收稿日期:2019-09-17
  • 最后修改日期:
  • 录用日期:
  • 在线发布日期: 2020-03-30
  • 出版日期: