中国农业科学 ›› 2012, Vol. 45 ›› Issue (7): 1399-1405.doi: 10.3864/j.issn.0578-1752.2012.07.019

• 兽医 • 上一篇    下一篇

利用PRNP-/-羊制备朊蛋白多克隆抗体及其特性分析

 王学斌, 俞慧清, 吴晓东, 徐旭俊, 陈建泉, 成国祥   

  1. 1.上海转基因研究中心,上海 201210
    2.上海杰隆生物工程股份有限公司,上海 201210
    3.中国动物卫生与流行病学中心, 青岛 266032,山东
  • 收稿日期:2011-11-22 出版日期:2012-04-01 发布日期:2012-02-06
  • 通讯作者: 通信作者陈建泉,E-mail:jqchen@cngenon.com
  • 作者简介:王学斌,Tel:021-51380636;E-mail:mars8558@126.com
  • 基金资助:

    国家转基因生物新品种培育重大专项(2009ZX08008-011B)、上海市科委研发基地建设项目(10dz2251700)

Production and Characterization of Anti-PrP Polyclonal Antibody by PRNP Gene Knockout Goat

 WANG  Xue-Bin, YU  Hui-Qing, WU  Xiao-Dong, XU  Xu-Jun, CHEN  Jian-Quan, CHENG  Guo-Xiang   

  1. 1.上海转基因研究中心,上海 201210
    2.上海杰隆生物工程股份有限公司,上海 201210
    3.中国动物卫生与流行病学中心, 青岛 266032,山东
  • Received:2011-11-22 Online:2012-04-01 Published:2012-02-06

摘要: 【目的】利用朊蛋白双基因敲除(PRNP-/-)羊制备朊蛋白多克隆抗体,并对其特性进行分析。【方法】构建山羊朊蛋白(PrP)原核表达载体,转入大肠杆菌并诱导表达,纯化获得羊PrP;将获得的PrP免疫PRNP-/-山羊,制备朊蛋白特异性的多克隆抗体;并对获得的朊蛋白多克隆抗体进行ELISA及Western-blot检测。【结果】获得了大量的朊蛋白特异性抗血清,间接ELASA检测抗血清中朊蛋白多克隆抗体的效价为25600;Western-blot检测显示所制备抗体不仅可以识别鼠、牛、羊脑组织内源性朊蛋白,而且能识别鼠脑组织内朊病毒。【结论】PRNP-/-转基因山羊可用于制备大量高亲和力朊蛋白多克隆抗体,获得的抗体可用于多种动物朊蛋白及朊病毒类疾病的检测。

关键词: 朊蛋白, 朊病毒, 多克隆抗体, 朊蛋白双基因敲除山羊

Abstract: 【Objective】The study was conducted in order to produce and characterize anti-PrP polyclonal antibodies by prion protein knockout (PRNP-/-) goat.【Method】Using polymerase chain reaction (PCR) method, the DNA sequence encoding the goat mature PrP (Prion Protein) was amplified from goat DNA. It was then cloned into the vector pET-22b to express recombinant PrP protein. After purification, the recombinant PrP was used as antigen to immunize PRNP-/- goat for producing anti-PrP antibodies. ELISA and Western blot were conducted to characterize the titer and specificity of polyclonal antibodies.【Result】A large scale of anti-PrP polyclonal antibodies was successfully produced by PRNP-/- goat. ELISA assay revealed that the titer of the polyclonal antibodies against PrP was as high as 1﹕25 600. Western blot test showed that the antibody was not only able to react with the native prion proteins (PrPC) of mouse, cattle and goat brain, but also could combine with misfolded prion proteins (PrPSc) from mouse brain.【Conclusion】Ablation of the prion protein(PrP) gene in goat facilitates the production of a large scale anti-PrP polyclonal antibodies, the produced antibody can be widely used in detecting PrPC and PrPSc derived from a variety of animals.

Key words: PrPC,  , PrPSc, polyclonal antibodies, PRNP-/- goat