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针对猪瘟病毒E2蛋白的嵌合猪源化单克隆抗体的表达及抗病毒活性鉴定
引用本文:陈姝承,孙慧敏,李素,刘平黄,马吉飞,仇华吉.针对猪瘟病毒E2蛋白的嵌合猪源化单克隆抗体的表达及抗病毒活性鉴定[J].生物工程学报,2017,33(8):1235-1243.
作者姓名:陈姝承  孙慧敏  李素  刘平黄  马吉飞  仇华吉
作者单位:1 天津农学院 动物科学与动物医学学院,天津 300384; 2 中国农业科学院哈尔滨兽医研究所,黑龙江 哈尔滨 150069,2 中国农业科学院哈尔滨兽医研究所,黑龙江 哈尔滨 150069,2 中国农业科学院哈尔滨兽医研究所,黑龙江 哈尔滨 150069,2 中国农业科学院哈尔滨兽医研究所,黑龙江 哈尔滨 150069,1 天津农学院 动物科学与动物医学学院,天津 300384,1 天津农学院 动物科学与动物医学学院,天津 300384; 2 中国农业科学院哈尔滨兽医研究所,黑龙江 哈尔滨 150069
基金项目:国家自然科学基金 (No. 31672537) 资助。
摘    要:猪瘟(Classical swine fever,CSF)是严重危害养猪业的一种烈性传染病,常造成巨大的经济损失,是世界动物卫生组织要求必须申报的动物疫病之一。猪瘟的病原是猪瘟病毒(Classical swine fever virus,CSFV),CSFV的结构蛋白由衣壳蛋白(C)和囊膜糖蛋白(E~(rns)、E1、E2)构成。E2蛋白是CSFV主要的保护性抗原,可以诱导机体产生中和抗体,从而抵抗CSFV的感染。此前,本团队制备了一株针对CSFV E2蛋白的鼠源单克隆抗体HQ06。文中将HQ06抗体重链和轻链可变区基因与猪源恒定区基因嵌合后克隆至真核表达载体,利用中国仓鼠卵巢(CHO)细胞制备一株针对CSFV E2蛋白的嵌合猪源化单克隆抗体c HQ06。应用ELISA、Western blotting试验证实了c HQ06与CSFV E2蛋白具有良好的反应性;中和试验结果表明c HQ06可以中和CSFV。综上所述,本研究应用CHO细胞稳定表达了具有良好反应性和中和活性的针对CSFV E2蛋白的嵌合猪源化单克隆抗体c HQ06,为研究CSFV E2蛋白结构、功能以及开发新型的CSFV诊断和治疗制剂奠定基础。

关 键 词:猪瘟病毒,单克隆抗体,基因工程抗体,嵌合表达,悬浮培养
收稿时间:2017/6/24 0:00:00

Expression and antiviral activity of a chimeric porcinized monoclonal antibody (cHQ06) against E2 protein of classical swine fever virus
Shucheng Chen,Huimin Sun,Su Li,Pinghuang Liu,Jifei Ma and Huaji Qiu.Expression and antiviral activity of a chimeric porcinized monoclonal antibody (cHQ06) against E2 protein of classical swine fever virus[J].Chinese Journal of Biotechnology,2017,33(8):1235-1243.
Authors:Shucheng Chen  Huimin Sun  Su Li  Pinghuang Liu  Jifei Ma and Huaji Qiu
Institution:1 College of Animal Science and Veterinary Medicine, Tianjin Agricultural University, Tianjin 300384, China; 2 Harbin Veterinary Research Institute, Chinese Academy of Agricultural Sciences (CAAS), Harbin 150069, Heilongjiang, China,2 Harbin Veterinary Research Institute, Chinese Academy of Agricultural Sciences (CAAS), Harbin 150069, Heilongjiang, China,2 Harbin Veterinary Research Institute, Chinese Academy of Agricultural Sciences (CAAS), Harbin 150069, Heilongjiang, China,2 Harbin Veterinary Research Institute, Chinese Academy of Agricultural Sciences (CAAS), Harbin 150069, Heilongjiang, China,1 College of Animal Science and Veterinary Medicine, Tianjin Agricultural University, Tianjin 300384, China and 1 College of Animal Science and Veterinary Medicine, Tianjin Agricultural University, Tianjin 300384, China; 2 Harbin Veterinary Research Institute, Chinese Academy of Agricultural Sciences (CAAS), Harbin 150069, Heilongjiang, China
Abstract:Classical swine fever (CSF), one of OIE-listed diseases, is a highly contagious and economically important disease of pigs. Classical swine fever virus (CSFV) is the causative agent of CSF. The capsid (C) protein and the glycoproteins Erns, E1 and E2, are structural components of the virus. E2 is the most immunogenic protein of the CSFV glycoproteins, inducing neutralizing antibodies that provide protection against lethal CSFV challenge. In a previous study, we developed a murine MAb HQ06 against the E2 protein of CSFV. In this study, the variable region genes from HQ06 and constant regions gene of swine antibody are fused and cloned into the eukaryotic expression vectors to establish a cell line which can stably express a chimeric porcinized MAb (cHQ06) against E2 in CHO cell. The purified cHQ06 antibody protein was determined to be successfully generated, which exhibited high reactivity between cHQ06 and the E2 protein of CSFV by enzyme-linked immunosorbent assay (ELISA) and Western blotting. More importantly, we investigated the neutralizing activity of cHQ06 against CSFV. In conclusion, this study generated cHQ06 for efficient and stable production which can be used against to develop novel diagnostic assays, investigate the structure and function of the E2 protein and generate novel preparations of diagnosis and treatment.
Keywords:classical swine fever virus  monoclonal antibody  genetic engineering antibody  chimeric expression  suspension culture
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