《中国畜牧兽医》 ›› 2019, Vol. 46 ›› Issue (7): 2144-2150.doi: 10.16431/j.cnki.1671-7236.2019.07.032

• 基础兽医 • 上一篇    下一篇

重组犬α6干扰素的酵母表达及其抗病毒活性评价

宋天琪1,2, 侯绍华1, 郭晓宇1, 鑫婷1, 姜一曈1, 袁维峰1, 朱鸿飞1, 贾红1   

  1. 1. 中国农业科学院北京畜牧兽医研究所, 北京 100193;
    2. 北京市通州区动物卫生监督所, 北京 101100
  • 收稿日期:2018-11-25 出版日期:2019-07-20 发布日期:2019-07-22
  • 通讯作者: 贾红 E-mail:jiahong80@126.com
  • 作者简介:宋天琪(1992-),女,内蒙古巴彦淖尔人,硕士,研究方向:预防兽医学,E-mail:462334021@qq.com
  • 基金资助:

    公益性行业(农业)科研专项经费项目(201303042);国家重点研发计划项目(2016YFD0501003)

Yeast Expression of Recombinant Canine Alpha Interferon 6 and Evaluation of Their Antiviral Activities

SONG Tianqi1,2, HOU Shaohua1, GUO Xiaoyu1, XIN Ting1, JIANG Yitong1, YUAN Weifeng1, ZHU Hongfei1, JIA Hong1   

  1. 1. Institute of Animal Sciences, Chinese Academy of Agricultural Sciences, Beijing 100193, China;
    2. Beijing Tongzhou District Animal Health Supervision, Beijing 101100, China
  • Received:2018-11-25 Online:2019-07-20 Published:2019-07-22

摘要:

试验旨在构建犬α6干扰素毕赤酵母表达系统,并对其进行优化和筛选,以期获得高活性的重组犬α6干扰素(CaIFN-α6)。根据CaIFN-α6基因序列,按毕赤酵母菌密码子偏好性对CaIFN-α6全基因序列进行优化与合成,用Xho Ⅰ和Not Ⅰ双酶切将其连接至载体pPICZαA中,构建pPICZαA-CaIFN-α6重组表达质粒,转化大肠杆菌DH5α感受态细胞。提取质粒pPICZαA-CaIFN-α6并线性化,电转入酵母感受态细胞X33中制备重组菌。采用甲醇进行诱导表达,收集上清,超滤浓缩,最终获得纯化的重组CaIFN-α6。利用BCA法测得纯化后的CaIFN-α6蛋白浓度为1.5 mg/mL,Western blotting分析表明CaIFN-α6蛋白具有良好的反应原性,SDS-PAGE显示其纯度约在95%以上,MDCK/VSV法检测其效价为2.37×107 IU/mL,比活性为1.58×107 IU/mg。结果表明犬α6干扰素在毕赤酵母pPICZαA表达载体系统中成功表达,且具有较高的生物活性,为后期的犬病毒病的临床预防与治疗提供了良好的支撑。

关键词: 犬α 6干扰素(CaIFN-α 6); 真核表达; 纯化; 抗病毒活性

Abstract:

The aim of the experiment was to construct the expression system of canine interferon alpha 6 (CaIFN-α6) in Pichia pastoris,optimize and screen the expression system in order to obtain recombinant canine interferon alpha 6 with high activity.According to the sequence of CaIFN-α6 gene and the codon preference of Pichia pastoris,the whole gene sequence of CaIFN-α6 was optimized and synthesized.The recombinant expression plasmid of pPICZαA-CaIFN-α6 was constructed using Xho Ⅰ and Not Ⅰ and linked to the vector pPICZαA.The recombinant expression plasmid was transformed into E.coli DH5α competent cells.The plasmid pPICZαA-CaIFN-α6 was extracted and linearized.The recombinant strain was prepared by electroporation into yeast competent cell X33.The recombinant CaIFN-α6 was purified by methanol induction,supernatant collection and ultrafiltration concentration.The concentration of purified CaIFN-α6 protein was 1.5 mg/mL by BCA.Western blotting analysis showed that CaIFN-α6 protein had good reactivity.SDS-PAGE showed that the purity of CaIFN-α6 protein was above 95%.The titer of CaIFN-α6 protein was 2.37×107 IU/mL by MDCK/VSV detection and the specific activity was 1.58×107 IU/mg.The results showed that CaIFN-α6 was successfully expressed in Pichia pastoris pPICZαA expression vector system with high biological activity,which provided a good support for the clinical prevention and treatment of canine viral disease in the later stage.

Key words: canine interferon alpha 6(CaIFN-α6); eukaryotic expression; purification; antiviral activity

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