中国畜牧兽医 ›› 2019, Vol. 46 ›› Issue (10): 3075-3083.doi: 10.16431/j.cnki.1671-7236.2019.10.030

• 预防兽医 • 上一篇    下一篇

牛分枝杆菌MPB70蛋白单克隆抗体的制备及检测

周曼莉1,2, 周玉成1, 张海威1, 乔连江1, 杨艳玲1   

  1. 1. 中国农业科学院特产研究所, 长春 130112;
    2. 宁夏大学, 西部特色生物资源保护与利用教育部重点实验室, 银川 750021
  • 收稿日期:2019-05-05 出版日期:2019-10-20 发布日期:2019-10-21
  • 通讯作者: 杨艳玲 E-mail:m18043213639@163.com
  • 作者简介:周曼莉(1994-),女,宁夏石嘴山人,硕士,研究方向:人兽共患病,E-mail:18195129796@163.com
  • 基金资助:
    “十三五”重点研发项目“牛羊重要病原分子诊断新技术”(2016YFD00500900);宁夏回族自治区重点研发计划项目(东西部合作)“牛羊重要传染病快速诊断与检测关键技术研究”(2017BN041)

Preparation and Detection of Monoclonal Antibodies Against Mycobacterium bovis MPB70 Protein

ZHOU Manli1,2, ZHOU Yucheng1, ZHANG Haiwei1, QIAO Lianjiang1, YANG Yanling1   

  1. 1. Institute of Special Animal and Plant Sciences of CAAS, Changchun 130112, China;
    2. Key Laboratory of Western Characteristic Biological Resources Protection and Utilization, Ministry of Education, Ningxia University, Yinchuan 750021, China
  • Received:2019-05-05 Online:2019-10-20 Published:2019-10-21

摘要: 为了制备牛分枝杆菌的单克隆抗体,本试验利用制备的原核表达的牛分枝杆菌重要抗原蛋白MPB70作为免疫原皮下多点注射免疫BALB/c小鼠。利用细胞融合技术,经过5次亚克隆与筛选,取已免疫好的小鼠脾细胞与SP2/0骨髓瘤细胞在PEG3500的作用下进行细胞融合。筛选得到了2株分泌抗牛分枝杆菌MPB70蛋白的杂交瘤细胞,分别命名为Anti-B-MPB70:8和Anti-B-MPB70:12。采用间接ELISA方法对获得的单克隆抗体进行亲和常数检测、效价分析及亚类鉴定,通过SDS-PAGE凝胶试验对单克隆抗体进行纯度分析,并检测其浓度,通过Western blotting方法对单克隆抗体的反应特性进行鉴定。结果显示,纯化后的MPB70蛋白分子质量大小为20 ku,浓度为0.5 mg/mL。两株单克隆抗体的亲和常数分别为9.95×109和9.53×108;抗体效价分别为1∶102 400和1∶12 800;抗体亚类分别为IgG2b和IgG1,轻链类型均为κ型;纯度>90%;浓度分别为3.0和2.2 mg/mL;且具有良好的反应特性。以上研究结果表明,本试验成功制备了抗MPB70蛋白单克隆抗体,可为牛结核病病原和抗体检测技术研究奠定基础。

关键词: 结核分枝杆菌; MPB70蛋白; 单克隆抗体

Abstract: In order to prepare monoclonal antibodies against Mycobacterium bovis(M.bovis),this experiment was carried out by immunizing BALB/c mice by subcutaneous injection of the prokaryotic expression of M.bovis important antigen protein MPB70.Using cell fusion technology,after 5 subclones and screening,the spleen cells of the well-immunized mice and the myeloma cells SP2/0 were subjected to cell fusion under the action of PEG3500.Two hybridoma cells secreting anti-M.bovis MPB70 protein were screened and named as Anti-B-MPB70:8 and Anti-B-MPB70:12,respectively.The indirect ELISA method was used to detect the affinity constant of the collected ascites,the titer analysis and the subclass identification.The purity of the monoclonal antibody was analyzed by SDS-PAGE test,the concentration of monoclonal antibodies was detected and the reaction characteristics of monoclonal antibodies were identified by Western blotting.The results showed that the purified MPB70 protein had a molecular mass of 20 ku and a concentration of 0.5 mg/mL.The affinity constants of the two monoclonal antibodies were 9.95×109 and 9.53×108,respectively;The antibody titers were 1:102 400 and 1:12 800,respectively;The antibody subclasses were IgG2b and IgG1,respectively,and the light chain types were κ type.The purity was greater than 90%;The concentrations were 3.0 and 2.2 mg/mL,respectively,and had good reactivity.The above results indicated that the monoclonal antibody against MPB70 protein had been successfully prepared,which could lay a foundation for the research of bovine tuberculosis pathogen and antibody detection technology.

Key words: Mycobacterium tuberculosis; MPB70 protein; monoclonal antibody

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