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抗东方马脑炎病毒结构蛋白E2单克隆抗体的制备及其抗原表位的鉴定
引用本文:赵晶,孙恩成,刘霓红,杨涛,杨银辉,耿宏伟,秦永丽,王凌凤,徐青元,吴东来.抗东方马脑炎病毒结构蛋白E2单克隆抗体的制备及其抗原表位的鉴定[J].中国预防兽医学报,2011,33(11).
作者姓名:赵晶  孙恩成  刘霓红  杨涛  杨银辉  耿宏伟  秦永丽  王凌凤  徐青元  吴东来
作者单位:1. 中国农业科学院哈尔滨兽医研究所兽医生物技术国家重点实验室 农业部兽医公共卫生重点开放实验室,黑龙江哈尔滨,150001
2. 军事医学科学院微生物流行病研究所病原微生物 生物安全国家重点实验室,北京,100071
基金项目:国家863项目,黑龙江省自然科学基因项目
摘    要:为制备抗东方马脑炎病毒(EEEV)结构蛋白E2的单克隆抗体(MAb)并鉴定其抗原表位,本研究以Bac-to-Bac真核表达系统表达EEEV E2蛋白,纯化后作为免疫原免疫BALB/c小鼠,取其脾淋巴细胞与小鼠骨髓瘤细胞SP2/0进行融合.以原核表达载体pET-30a表达并纯化的EEEV E2蛋白作为包被抗原建立间接ELISA方法筛选杂交瘤细胞,获得4株稳定分泌抗EEEV E2蛋白MAbs的杂交瘤细胞株,分别命名为6F3、6F11、7C11、8B11.Western blot与间接免疫荧光试验结果表明,获得的4株MAbs均与EEEV呈阳性反应,而与西方马脑炎病毒、乙型脑炎病毒以及登革热病毒1型~4型呈阴性反应.利用部分重叠的原核表达的短肽对E2蛋白抗原表位进行鉴定,初步确定MAb 6F11、7C11和8B11识别的抗原表位均为E-33 (321EGLEYTWGNHPPKRVW336),而MAb 6F3无短肽与其反应,推测可能为构象表位.本研究结果为建立EEEV型特异性检测方法、研究E2蛋白结构功能及该病的进一步防制奠定了基础.

关 键 词:东方马脑炎病毒  E2蛋白  原核表达  真核表达  单克隆抗体  抗原表位

Preparation of monoclonal antibodies against eastern equine encephalitis virus E2 protein and the B-cell epitopes identification
ZHAO Jing,SUN En-cheng,LIU Ni-hong,YANG Tao,YANG Yin-hui,GENG Hong-wei,QIN Yong-li,WANG Ling-feng,XU Qing-yuan,WU Dong-lai.Preparation of monoclonal antibodies against eastern equine encephalitis virus E2 protein and the B-cell epitopes identification[J].Chinese Journal of Preventive Veterinary Medicine,2011,33(11).
Authors:ZHAO Jing  SUN En-cheng  LIU Ni-hong  YANG Tao  YANG Yin-hui  GENG Hong-wei  QIN Yong-li  WANG Ling-feng  XU Qing-yuan  WU Dong-lai
Institution:ZHAO Jing1,SUN En-cheng1,LIU Ni-hong1,YANG Tao1,YANG Yin-hui2,GENG Hong-wei1,QIN Yong-li1,WANG Ling-feng1,XU Qing-yuan1,WU Dong-lai1(1.Key Laboratory of Veterinary Public Health of Ministry of Agriculture,State Key Laboratory of Veterinary Biotechnology,Harbin Veterinary Research Institute,Chinese Academy of Agricultural Sciences,Harbin 150001,China,2.Institute of Microbiology and Epidemiology,Academy of Military Medical Sciences,Beijing 100071,China)
Abstract:For preparation of monoclonal antibodies(MAb) against eastern equine encephalitis virus(EEEV) structural glycoprotein E2 and identification of the B-cell epitopes,BALB/c mice were immunized with protein E2 expressed in Bac-to-Bac eukaryotic expression system.Splenocytes of the BALB/c mice were fused with myeloma cell SP2/0 for producing hybridoma.Four hybridomas stably secreting MAbs against the protein E2 were developed,designated 6F3,6F11,7C11 and 8B11,and determined by indirect ELISA,coating with purifie...
Keywords:eastern equine encephalitis virus  E2 protein  prokaryotic expression  eukaryotic expression  monoclonal antibody  epitopes  
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