期刊文献+

猪链球菌WC-SS7株GDH基因的表达及GDH蛋白单克隆抗体的制备 被引量:4

Expression of GDH gene of Streptococcus suis and preparation of monoclonal antibody against GDH protein
下载PDF
导出
摘要 目的原核表达猪链球菌7型临床分离株WC-SS7的GDH蛋白,制备抗GDH蛋白的单克隆抗体(mAb)。方法将临床分离的猪链球菌7型WC-SS7株的GDH基因克隆入表达载体pET-30a,转入大肠杆菌中,用IPTG诱导表达,用Ni化琼脂糖柱(Pierce)纯化的GDH蛋白免疫BALB/c小鼠,取鼠脾细胞与SP2/0骨髓瘤细胞融合,通过间接ELISA方法筛选阳性克隆,对抗WC-SS7GDH蛋白单克隆抗体进行特异性鉴定及亚型鉴定。结果表达产物经SDS-PAGE凝胶电泳分析后,在约为52KD处可见一条明显的诱导表达带,说明GDH蛋白得到了正确的表达;细胞融合后检测为阳性的细胞株经过3次单克隆筛选,最终得到了6株能和GDH蛋白反应的能稳定分泌单抗的阳性细胞克隆,这些单抗通过Western鉴定结果显示其具有良好的特异性,6株单克隆抗体亚型鉴定结果显示其亚型均为IgG1型,且轻链均为κ链。结论本研究成功表达了WC-SS7的GDH蛋白,并获得了6株能和GDH蛋白反应的、能稳定分泌单抗的阳性细胞克隆,所获得的重组GDH蛋白及特异性单克隆抗体能用于猪链球菌结构和功能的研究,为猪链球菌临床感染血清学诊断方法的建立奠定基础。 In order to express GDH protein of Streptococcus suis in prokaryotic cell and produce monoclonal antibody (mAb) against GDH protein. The GDH gene of Streptococcus suis strain of WC SS7 was truncated and cloned into prokaryotic expression vector PET 30(a), expressed in E. coli after IPTG induction. Expressed fusion protein was purified by Ni-NTA, BALB/c mice were immunized with purified GDH protein. Murine myeloma cells were fused with the splenoeytes of the immunized mice after the third immunization. An indirect ELISA coated with GDH was used to screen Hybridomas for production of specific antibody in hybridoma culture fluid. The specificity of these mAbs were characterized by western-blot. These mAbs were subtyped by ELISA using a commercial kit. The result showed that fusion protein of 52KD was expressed by SDS-PAGE analysis, 6 hybridomas clones producing mAbs steadily were obtained after 3 cycles of cloning. The specificity of These mAbs were conformed by western blot. All the mAbs belong to IgG1 subtype, and the light chains of the antibodies are k chain. The purified GDH protein of streptococcus suis and 6 hybridomas clones producing mAbs steadily were successfully obtained. The anti GDH mAbs obtained has strong specificity and high tilter, which and GDH protein could be used for further analysis of the structure and function of .Streptococcus suis and lay the foundation for diagnosis assays to serology of Streptococcus suis clinical infection.
出处 《中国人兽共患病学报》 CAS CSCD 北大核心 2009年第10期980-983,共4页 Chinese Journal of Zoonoses
基金 国家973计划(2006CB504401)
关键词 猪链球菌 GDH蛋白 原核表达 单克隆抗体 Streptococcus suis GDH protein prokaryotic expression monoclonal antibody
  • 相关文献

参考文献11

  • 1Bartelink A K M , E van Kregten. Streptococcus suis as threat to pig farmers and abattoir workers [J]. Thelancet , 1995 , 346 (8991-8992) : 1707. 被引量:1
  • 2Berthelot Herauh F , Morvan H , Keribin AM , et al . Production of muraminidase released protein (MRP), extracellular factor (EF) and suilysin by field isolates of Streptococcus suis capsular types 2, 1/2, 9, 7 and 3 isolated from swine in France[J]. Vet Res,2000,31(5) :473-479. 被引量:1
  • 3张晶,吴华伟,陈征.人兽共患病原菌-猪链球菌2型的发病特点与防治对策[J].中国兽药杂志,2007,41(9):38-40. 被引量:6
  • 4Okwumabua O, Persaud JS, Reddy PG. Cloning and characterization of the gene encoding the glutamate dehydrogenase of Streptococcus suis serotype 2 (J). Clin Diagn Lab Immunol, 2001, 8(2): 251-257. 被引量:1
  • 5段小莉,黄文晋,王百忍,宋俊峰,金卫林,郭翔,鞠躬.GAP-43原核表达载体的构建、表达及抗GAP-43单克隆抗体的制备[J].细胞与分子免疫学杂志,2003,19(5):480-482. 被引量:3
  • 6程海霞,曹江,沈建根,郑树.GST-HAI-1融合蛋白的表达及抗人HAI-1单克隆抗体的制备[J].生物工程学报,2004,20(4):496-500. 被引量:4
  • 7Kohler G, Milstein C. Continuous cultures of fused cells secrering antibody of predefined specificity(J). Nature, 1975, 20(3) : 495-497. 被引量:1
  • 8Kearney J F, Radbruch A, Liesegang B,et al. A new mouse myeloma cell line that has lost immune globulin expression but permits the construction of antibody secreting hybrid cell lines[J]. J Immunol, 1979,23,p. 1548-1550. 被引量:1
  • 9Grunow R, Giese R, Porstmann T, etal. Development and biological testing of human and murine monoclonal antibodies against HIV antiGDHns(J). Z Klin Med,1990,5,p. 367-369. 被引量:1
  • 10Baggio L, Morrison M. The NAD(P)H utilizing Glutamate Dehydrogenase of Baeteroides thetaiotaomicron Belongs to Enzyme family Ⅰ, and its activity is affected by tras-acting genes positioned downstream of gdhA(J). J Baeteriol 1996, 178 (24): 7212-20. 被引量:1

二级参考文献42

共引文献9

同被引文献35

引证文献4

二级引证文献8

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部