检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:潘娜[1] 石琳[1] 黄丽华[1] 周立[1] 何大水[1] 张宇光[1]
机构地区:[1]中国医学科学院中国协和医科大学血液学研究所,天津300020
出 处:《细胞与分子免疫学杂志》2007年第7期652-656,共5页Chinese Journal of Cellular and Molecular Immunology
摘 要:目的:联合应用DNA免疫和细胞抗原加强制备抗DAF单克隆抗体(mAb)并鉴定其特性。方法:利用分子克隆的方法构建重组质粒pcDNA3.1/DAF。以其免疫BALB/c小鼠股四头肌3次,并在融合前用表达DAF分子的HPB-ALL细胞为抗原加强免疫1次,制备抗DAFmAb。以ELISA法测定mAb的Ig亚类。采用流式细胞术和Westernblot鉴定mAb的特异性和结合活性。以非免疫竞争法测定mAb的亲和常数。结果:成功地获得2株可识别DAF分子不同抗原表位的mAbB6E和2B6B,其Ig亚类均为IgG2a。mAb2B6E的亲和常数为1.81×10-7mol/L,与天然的细胞膜蛋白、变性的膜蛋白以及重组DAF蛋白都有良好的结合活性和特异性。结论:先以pcDNA3.1/DAF肌肉内免疫,再应用细胞抗原加强免疫的方法制备特异性的mAb,为在无法获得纯化蛋白质的情况下开拓了研制特异性抗体的新途径,也为日后改造抗DAFmAb进行靶向治疗研究打下了基础。AIM: To produce mAb against DAF by DNA immunization followed by a single boost with cell antigen and to characterize its property. METHODS: Recombinant plasmid pcDNA3. 1/DAF was constructed by molecular cloning technique and injected into mice quadriceps muscle of thigh. To boost the DAF immunized mice, HPB-AII cell antigen were injected on day 3 before cell fusion. The affinity and property of mAb to natural membrane protein and denatured protein were identified by FCM, fluorescence microscope and Westem blot. RESULTS: Two mAb against DAF were obtained, namely 2B6B and 2B6E. The affinity constant of 2B6E was 1.81 × 10^-7 mol/L. The isotype of the two mAbs were IgG2a, and the epitope of them was different. FCM, fluorescence microscope and Western blot indicated that the obtained mAb had affinity to natural membrane protein and denatured protein with high specificity. CONCLUSION: This study indicates that the DNA immunization and cell antigen boost method enables mice to produce mAb against DAF. The low frequency of nonspecific mAb is one of the advantages of this method compared to the conventional cell immunization method . Moreover the mAb generated by this method has satisfactory binding activity and specificity.
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:216.73.216.28