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A组猪轮状病毒NSP3蛋白单克隆抗体的制备及抗原表位鉴定 被引量:1

Preparation of monoclonal antibody against NSP3 protein of group A porcine rotavirus and identification of antigenic epitopes
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摘要 为制备A组猪轮状病毒(Po RV)非结构蛋白NSP3的单克隆抗体(MAb)及鉴定其抗原表位,本研究将原核表达、纯化的重组NSP3蛋白(r NSP3)免疫BALB/c小鼠,取免疫小鼠的脾细胞与SP2/0细胞进行融合,经间接ELISA法筛选,得到一株能够稳定分泌抗Po RV(G9)的杂交瘤细胞株(5B8)。MAb鉴定结果显示其抗体亚类为Ig G1型;MAb细胞培养上清液效价为1∶103,western blot及间接免疫荧光结果表明该株MAb能够与Po RV反应。对NSP3蛋白进行截短表达,采用western blot试验确定所获得的MAb识别的抗原表位区域序列为290QDYD RTFL297。该MAb的制备为进一步研究NSP3蛋白的结构和功能奠定了良好的基础。 To prepare the monoclonal antibody (MAb) against NSP3 of porcine group A rotavirus (PoRV) and identify epitope in NSP3, the NSP3 gene was cloned to pGEX-6P-1 vector and the recombinant NSP3 was expressed in E.coli as antigen and immune to the mice. Then, one hybridoma stably secreting MAb against NSP3 protein was prepared by fusing SP2/0 cells with spleen cells from BALB/c mice, and identified by indirect ELISA. The MAb belonged to IgG1 subtype. The titer in cell culture medium of the hybridomas reach to 1:10^3. In addition, the MAb was positively reacted with authentic NSP3 protein of PoRV verified by the western blot and indirect irnmunofluorescence assay. To identify the antigenic epitope against this MAb, a series of truncated NSP3 protein were expressed in E.coli and detected with the MAb by western blot method. The linear epitope sequence of ^290 QDYDRTFL^297 in NSP3 protein was identified, Those results provided a basis for the further study on the structure and function of the NSP3.
出处 《中国预防兽医学报》 CAS CSCD 北大核心 2015年第4期295-298,共4页 Chinese Journal of Preventive Veterinary Medicine
基金 黑龙江省高等学校科技创新团队项目(2011TD001)
关键词 A组猪轮状病毒 NSP3蛋白 单克隆抗体 抗原表位 porcine group A rotavirus NSP3 pretein monoclonal antibody antigenic epitope
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参考文献12

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