中国畜牧兽医 ›› 2020, Vol. 47 ›› Issue (8): 2660-2665.doi: 10.16431/j.cnki.1671-7236.2020.08.036

• 基础兽医 • 上一篇    下一篇

猪圆环病毒3型新疆株Cap蛋白的原核表达及纯化

谷思颖1, 屈勇刚1, 魏其1, 吴圆圆1, 于会举1, 李岩2   

  1. 1. 石河子大学动物科技学院, 石河子 832003;
    2. 新疆生产建设兵团畜牧兽医工作总站, 乌鲁木齐 830063
  • 收稿日期:2020-02-23 出版日期:2020-08-20 发布日期:2020-08-15
  • 通讯作者: 屈勇刚, 李岩 E-mail:quyonggang@shzu.edu.cn;bt4641862@163.com
  • 作者简介:谷思颖(1996-),女,新疆乌鲁木齐人,硕士生,研究方向:预防兽医,E-mail:1437919680@qq.com
  • 基金资助:
    国家自然科学基金"新疆重要自然宿主和媒介昆虫携带人兽共患病毒的病原生态学与分子流行病学研究"(U1503283)

Prokaryotic Expression and Purification of Cap Protein of Xinjiang Porcine Circovirus Type 3 Strain

GU Siying1, QU Yonggang1, WEI Qi1, WU Yuanyuan1, YU Huiju1, LI Yan2   

  1. 1. College of Animal Science and Technology, Shihezi Univerisity, Shihezi 832003, China;
    2. The General Station of Animal Husbandry and Veterinary Medicine of Xinjiang Production and Construction Corps, Urumqi 830063, China
  • Received:2020-02-23 Online:2020-08-20 Published:2020-08-15

摘要: 本研究旨在通过构建pGEX-4T-1-Cap原核表达载体,制备猪圆环病毒3型(PCV3)重组核衣壳(Cap)蛋白抗原。将密码子优化的PCV3 Cap全基因插入pGEX-4T-1载体,构建重组质粒pGEX-4T-1-Cap,转化大肠杆菌BL21(DE3)感受态细胞中,筛选出最佳诱导条件,通过谷胱甘肽琼脂糖树脂纯化重组Cap蛋白。结果表明,成功构建重组质粒pGEX-4T-1-Cap;在IPTG终浓度为0.1 mmol/L、16 ℃诱导20 h的条件下,可获得大量可溶性重组Cap蛋白,SDS-PAGE结果表明分子质量在51.6 ku,与预期相符;Western blotting分析表明经纯化的Cap蛋白与鼠抗GST单克隆抗体、PCV3兔源阳性血清呈阳性反应,进一步证实了重组蛋白的表达。本研究表达并纯化了PCV3 Cap重组蛋白,为新型基因工程亚单位疫苗的研制和ELISA血清学诊断方法的建立奠定了基础。

关键词: 猪圆环病毒3型(PCV3); Cap蛋白; 原核表达; 蛋白纯化

Abstract: The purpose of this study was to prepare porcine circovirus type 3 (PCV3) capsid protein by construct a prokaryotic expression vector pGEX-4T-1-Cap.Recombinant plasmid pGEX-4T-1-Cap was constructed by inserting codon optimized PCV3 Cap gene into pGEX-4T-1 vector,and then transformed into Escherichia coli BL21 (DE3) competent cell.The optimal induction conditions were screened out,and the recombinant Cap protein was purified by glutathione agarose resin.The results showed that the recombinant plasmid pGEX-4T-1-Cap was successfully constructed.A large amount of soluble recombinant capsid protein could be obtained under the condition that the final concentration of IPTG was 0.1 mmol/L and induced at 16 ℃ for 20 h.SDS-PAGE results showed that the molecular mass of the recombinant capsid protein was 51.6 ku with the same size as expected.Western blotting analysis showed that the purified Cap protein reacted positively with mouse anti-GST monoclonal antibody and PCV3 rabbit-derived positive serum,further confirming the expression of the recombinant protein.Therefore,the recombinant protein PCV3 Cap expressed and purified in this study,it laid a foundation for the development of new gene engineering subunit vaccine and the establishment of ELISA method.

Key words: porcine circovirus type 3(PCV3); capsid protein; prokaryotic expression; protein purification

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