[口蹄疫病毒118蛋白单克隆抗体的制备、鉴定及应用]。

Bin Xiao, Wenbo Hao, Zhenglun Du, Xiaoqing Liao, Shuhong Luo
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引用次数: 0

摘要

本实验旨在制备抗Orf病毒118蛋白的单克隆抗体,并利用该抗体研究ORFV118的生物学特性。构建了含有ORFV118全长基因的重组质粒pET33b-ORFV118。将质粒转化到大肠杆菌BL21中,用异丙基-β-d-硫代半乳糖苷(IPTG)诱导ORFV118表达。原核ORFV118通过Ni-NTA亲和层析纯化,随后作为抗原免疫小鼠。利用杂交瘤技术制备抗orfv118抗体。采用间接ELISA法和Western blot/免疫组化法分别检测该抗体的效价和特异性。我们成功地获得了三种抗体分泌杂交瘤,1A2,3B5和5D10。3株杂交瘤的效价分别为1:10000、1:6400和1:8000。选择单克隆抗体(mAb)、1A2和最高效价进行进一步研究。IgG1型抗体mAb 1A2与真核和天然ORFV118免疫抗原结合,具有高特异性。免疫组化分析显示局灶特异性染色仅限于表皮层和皮下组织,符合ORFV感染的特征。mAb 1A2以高特异性识别orfv118。进一步研究mAb 1A2将有助于我们了解ORFV118,并为Orf的诊断、预防和治疗提供潜在的新方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Preparation,Identification,and Application of Monoclonal Antibody against Orf Virus 118 Protein].

This study was designed to prepare a monoclonal antibody against Orf virus 118 protein and explore the biological properties of ORFV118 using this antibody. We constructed a recombinant plasmid pET33b-ORFV118 that contained a full-length ORFV118 gene. The plasmid was transformed into E.coli BL21,and the expression of ORFV118 was induced by isopropyl-β-d-thiogalactoside (IPTG).Prokaryotic ORFV118 was purified via Ni-NTA affinity chromatography and was subsequently used as an antigen to immunize mice. An anti-ORFV118 antibody was prepared using hybridoma technology. The titer and specificity of this antibody were tested by an indirect ELISA and Western blot/immunohistochemistry, respectively. We successfully obtained three antibody-secreting hybridomas,1A2,3B5,and 5D10.The titers of the three hybridomas were 1:10000,1:6400,and 1:8000.The monoclonal antibody (mAb),1A2 and the highest titer was selected for further research. The mAb 1A2,an IgG1 type antibody was bonded to its immunizing antigen, both the eukaryotic and natural ORFV118 with high specificity. The immunohistochemical analysis showed that the focal specific staining was restricted to the epidermal layer and subcutaneous tissue, which conformed to the characteristics of an ORFV infection. The mAb 1A2 recognized ORFV118with high specificity. Further study of mAb 1A2 will facilitate our understanding of ORFV118 and provide potentially novel methods for the diagnosis, prevention, and treatment of Orf.

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