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王磊, 胡骁飞, 滕蔓, 王耀, 孙亚宁, 裴亚峰, 张改平, 邓瑞广. 抗黄曲霉毒素B1单抗制备及免疫学定量方法建立[J]. 中国公共卫生, 2012, 28(1): 58-60. DOI: 10.11847/zgggws2012-28-01-24
引用本文: 王磊, 胡骁飞, 滕蔓, 王耀, 孙亚宁, 裴亚峰, 张改平, 邓瑞广. 抗黄曲霉毒素B1单抗制备及免疫学定量方法建立[J]. 中国公共卫生, 2012, 28(1): 58-60. DOI: 10.11847/zgggws2012-28-01-24
WANG Lei, HU Xiao-fei, TENG Man, . Development of monoclonal antibody against Aflatoxin B1 and establishment of immunology quantitative ELISA[J]. Chinese Journal of Public Health, 2012, 28(1): 58-60. DOI: 10.11847/zgggws2012-28-01-24
Citation: WANG Lei, HU Xiao-fei, TENG Man, . Development of monoclonal antibody against Aflatoxin B1 and establishment of immunology quantitative ELISA[J]. Chinese Journal of Public Health, 2012, 28(1): 58-60. DOI: 10.11847/zgggws2012-28-01-24

抗黄曲霉毒素B1单抗制备及免疫学定量方法建立

Development of monoclonal antibody against Aflatoxin B1 and establishment of immunology quantitative ELISA

  • 摘要: 目的本研究合成并鉴定了AFB1人工抗原,制备AFB1的单克隆抗体(AFB1mAb)。方法采用NHS法将AFB1分别偶联于载体蛋白BSA和OVA上,分别合成W人工抗原AFB1-BSA和AFB1-OVA,紫外分光光度法和SDS-PAGE进行鉴定;AFB1-BSA免疫BALB/C小鼠,通过间接ELISA和阻断ELISA法选择细胞融合备用鼠;用杂交瘤技术制备AFB1mAb,并对其效价、亲和力、敏感性、特异性、亚型进行鉴定;体内诱生腹水法大量制备单抗。结果 UV图谱和SDS-PAGE图表明结半抗原AFB1和载体BSA及OVA偶联成功;筛选出2H5-F6、2H5-C9、2H9-C3三株杂交瘤细胞;鉴定单抗亚型均为IgG1;细胞上清效价1:2.0×102~1:1.28×103,2H5-F6的腹水效价1:1.28×106,AFB1mAb亲和常数Ka为2.65×1010 L/moL,对AFB1的IC50为2.58 ng/mL;与AFB2的交叉反应率为1.61%,与其他类药物无交叉反应。结论通过试验获得高效价、敏感、特异的AFB1mAb,可用于各种食品中AFB1残留的快速免疫学检测试验。

     

    Abstract: ObjectiveThe goal of this study was to synthesize artificial antigen of AFB1,to prepare monclonal antibody against AFB1.MethodsImmunogen AFB1-BSA and coating antigen AFB1-OVA were synthesized using NHS by linking carrier proteins BSA and OVA to AFB1 and identified by ultraviolet scanning,SDS-PAGE.BALB/C mice were immunized with AFB1-BSA,The titre and sensitivity of polyclonal antibody was detected by indirect ELISA and blocking ELISA,so as to select the mouse used in cell fusion.AFB1 mAb was prepared by hybridoma technology.The titer,affinity, sensitivity,specificity and subtype of the mAb were characterized.Massive AFB1 mAb were induced from in vivo method.ResultsThe results showed that the hapten AFB1 was successfully linked to carrier proteins by the UV scanning spectrum and SDS-PAGE electrophoresis.There hybridoma cell lines of 2H5-F6、2H5-C9、2H9-C3 were screened for specificity to AFB1,all the isotypes of the mAb were IgG1.The indirect ELISA titer of the mAb were 1:2.0×102~1:1.28×103 in supernatant,1:1.28×106 of 2H5-F6 in ascites,and the affinity constant(Ka)was 2.65×1010 L/moL,the mAb of 2H5-F6 show ed good sensitivity with IC50 of 2.58 ng/mL to AFB1.The rate of cross reaction of AFB1 mAb with AFB2 was 1.61%, and there was no cross-reactivity to other compounds.ConclusionAFB1 mAb of high-titer,sensitivity and specificity had been generated,it is possible to establish immunoassay of AFB1 residues in food.

     

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