中国畜牧兽医 ›› 2023, Vol. 50 ›› Issue (5): 1959-1970.doi: 10.16431/j.cnki.1671-7236.2023.05.023

• 预防兽医 • 上一篇    下一篇

猪源戊型肝炎病毒ORF2蛋白生物信息学分析及真核表达研究

卓娜1, 朱忠武3, 李静2, 胡世享1, 王建昌4, 林华5, 陈朝林1, 韩佃刚2, 艾军2, 陈培富1   

  1. 1. 云南农业大学, 昆明 651000;
    2. 云南昆明海关技术中心, 昆明 651000;
    3. 湖南长沙海关技术中心, 长沙 410000;
    4. 河北石家庄海关技术中心, 石家庄 050000;
    5. 四川成都海关技术中心, 成都 610000
  • 收稿日期:2022-08-29 出版日期:2023-05-05 发布日期:2023-04-28
  • 通讯作者: 艾军, 陈培富 E-mail:52563122@qq.com;cltwins2003@163.com
  • 作者简介:卓娜,E-mail:2625800300@qq.com。
  • 基金资助:
    国家重点研发计划课题(2022YFC2601605);云南省技术创新人才(2016HB018);云南省院士工作站

Bioinformatics Analysis and Eukaryotic Expression of ORF2 Protein of Swine Hepatitis E Virus

ZHUO Na1, ZHU Zhongwu3, LI Jing2, HU Shixiang1, WANG Jianchang4, LIN Hua5, CHEN Chaolin1, HAN Diangang2, AI Jun2, CHEN Peifu1   

  1. 1. Yunnan Agricultural University, Kunming 651000, China;
    2. Yunnan Kunming Customs Technology Center, Kunming 651000, China;
    3. Hunan Changsha Customs Technology Center, Changsha 410000, China;
    4. Hebei Shijiazhuang Customs Technology Center, Shijiazhuang 050000, China;
    5. Sichuan Chengdu Customs Technology Center, Chengdu 610000, China
  • Received:2022-08-29 Online:2023-05-05 Published:2023-04-28

摘要: 【目的】分析猪源戊型肝炎病毒(Swine hepatitis E virus,sHEV)4型ORF2蛋白的结构和功能,筛选具有保护性抗原的基因片段并表达蛋白,为研究其作为潜在保护性抗原提供候选蛋白。【方法】对sHEV 4型ORF2蛋白进行生物信息学分析,选取具有潜在保护性抗原蛋白的基因片段ORF2(128/140),通过PCR扩增、酶切后克隆至昆虫细胞表达载体,转染sf9细胞,通过Western blotting鉴定分析表达蛋白p128/p140。【结果】生物信息学分析显示,sHEV 4型ORF2蛋白存在2个稳定蛋白:p128和p140,分别含有496和476个氨基酸,二者皆为稳定蛋白,无跨膜区,蛋白二级结构主要以无规则卷曲为主。p128蛋白有11个T细胞表位、21个B细胞表位;p140蛋白有14个T细胞表位、18个B细胞表位。成功构建ORF2(128)、ORF2(140)2个基因的昆虫细胞表达载体,转染sf9细胞后经Western blotting检测发现,表达蛋白可被His标签单抗、sHEV抗体阳性血清识别。【结论】试验发现2个sHEV具有潜在保护性抗原的p128和p140蛋白,均可在sf9细胞中表达,且具有免疫活性。结果为进一步研究sHEV ORF2蛋白的功能和新型疫苗的研发提供了材料。

关键词: 猪戊型肝炎病毒(sHEV); ORF2蛋白; 生物信息学分析; 昆虫细胞; 表达

Abstract: 【Objective】 The purpose of this study was to analyze the structure and function of ORF2 protein of Swine hepatitis E virus (sHEV) genotype 4,screen the gene fragment with protective antigen and express,so as to provide a candidate protein for the study of its potential protective antigen.【Method】 The bioinformatics analysis of sHEV genotype 4 ORF2 protein was carried out.The gene fragment ORF2 (128/140) with potential protective antigen protein was selected,amplified by PCR and digested,which cloned into insect cell expression vector,and transfected into sf9 cells.The expressed protein p128/p140 were analyzed by Western blotting.【Result】 Bioinformatics analysis showed that the ORF2 protein of sHEV genotype 4 had two stable proteins (p128 and p140),which contained 496 and 476 amino acids,respectively.Both of them were stable proteins,without transmembrane regions,and the secondary structure of the protein was mainly random coil.p128 protein had 11 T cell epitopes and 21 B cell epitopes,and p140 protein had 14 T cell epitopes and 18 B cell epitopes.Insect cell expression vector of ORF2(128) and ORF2(140) genes were successfully constructed,and transfected into sf9 cells,Western blotting results showed that the expressed proteins could be recognized by His-tag monoclonal antibody and positive serum of sHEV antibody.【Conclusion】 p128 and p140 proteins with potential protective antigen of sHEV were found in this study,and the two proteins were expressed in sf9 cells with immune activity,which provide materials for further study of the function of sHEV ORF2 protein and the development of new vaccines.

Key words: Swine hepatitis E virus (sHEV); ORF2 protein; bioinformatics analysis; insect cell; expression

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