Pan Na, Shi Lin, Huang Li-hua, Zhou Li, He Da-shui, Zhang Yu-guang
Department of Immunology, Institute of Hematology and Blood Diseases Hospital, Chinese Academy of Medical Sciences Peking Union Medical College, Tianjin 300020, China.
Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi. 2007 Jul;23(7):652-6.
To produce mAb against DAF by DNA immunization followed by a single boost with cell antigen and to characterize its property.
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-All 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 Western blot.
Two mAb against DAF were obtained, namely 2B6B and 2B6E. The affinity constant of 2B6E was 1.81x10(-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.
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.
通过DNA免疫,随后用细胞抗原进行单次加强免疫来制备抗衰变加速因子(DAF)的单克隆抗体(mAb),并对其特性进行表征。
采用分子克隆技术构建重组质粒pcDNA3.1/DAF,并将其注射到小鼠大腿股四头肌中。为加强DAF免疫的小鼠,在细胞融合前3天注射HPB-All细胞抗原。通过流式细胞术(FCM)、荧光显微镜和蛋白质印迹法鉴定mAb对天然膜蛋白和变性蛋白的亲和力及特性。
获得了两种抗DAF的mAb,即2B6B和2B6E。2B6E的亲和常数为1.81×10⁻⁷mol/L。这两种mAb的亚型均为IgG2a,且它们的表位不同。FCM、荧光显微镜和蛋白质印迹法表明,所获得的mAb对天然膜蛋白和变性蛋白具有亲和力,且特异性高。
本研究表明,DNA免疫和细胞抗原加强免疫方法能使小鼠产生抗DAF的mAb。与传统细胞免疫方法相比,非特异性mAb频率低是该方法的优点之一。此外,通过该方法产生的mAb具有令人满意的结合活性和特异性。