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抗重金属汞离子抗体的制备及鉴定
引用本文:赵丽,王凤龙,杨慧,李鹏,刘满杏,李霞.抗重金属汞离子抗体的制备及鉴定[J].生物工程学报,2010,26(6):753-759.
作者姓名:赵丽  王凤龙  杨慧  李鹏  刘满杏  李霞
作者单位:1. 内蒙古农业大学动物科学与医学学院,呼和浩特010018;北京市农林科学院蔬菜研究中心,北京100097
2. 内蒙古农业大学动物科学与医学学院,呼和浩特,010018
3. 北京市农林科学院蔬菜研究中心,北京,100097
4. 北京市农林科学院蔬菜研究中心,北京100097;北京农产品质量检测与农田环境监测技术研究中心,北京100097
基金项目:国家高技术研究发展计划 (863计划) (No. 2007AA10Z439),国家自然科学基金 (No. 30671205),北京市科委课题 (No. Z09090501040901) 资助。
摘    要:汞、镉、铅等重金属引起的环境污染已在世界范围内造成危害。快速、廉价地监测生境中重金属是减小其对人类及动物危害的先决条件。传统检测方法无法满足高通量的现场检测,建立更快速、更经济的免疫分析法检测汞离子是生产及经济发展的需要。本研究中,报道了汞特异性单克隆抗体的制备与筛选方法和结果。因Hg2+太小以至于不能引起免疫反应,所以用螯合剂(二乙烯三胺五乙酸,DTPA)将金属离子与载体蛋白(匙孔血蓝蛋白,KLH)连接起来。成功合成、鉴定汞复合物抗原后,免疫BALB/c小鼠,通过细胞融合获得了稳定分泌抗体的杂交瘤细胞。用极限稀释法亚克隆,通过ELISA筛选,获得了2株稳定分泌抗汞离子抗体的细胞株(H2H5,H1H8)。小鼠腹腔注射1×107H2H5、H1H8细胞株制备腹水,腹水抗体效价都在1∶51200以上。经鉴定两株杂交瘤均为IgG1亚类,轻链为kappa型且分泌抗体稳定性较好。实验结果为汞离子残留免疫学检测方法的建立提供了技术基础,对提高风险评估工作的效率和质量,保障食品安全有重要现实意义。

关 键 词:汞,螯合抗原,单克隆抗体,酶联免疫吸附法
收稿时间:2009/12/29 0:00:00

Preparation and characterization of specific monoclonal antibodies against mercury ions
Li Zhao,Fenglong Wang,Hui Yang,Peng Li,Manxing Liu and Xia Li.Preparation and characterization of specific monoclonal antibodies against mercury ions[J].Chinese Journal of Biotechnology,2010,26(6):753-759.
Authors:Li Zhao  Fenglong Wang  Hui Yang  Peng Li  Manxing Liu and Xia Li
Institution:College of Animal Science and Medicine, Inner Mongolia Agricultural University, Hohhot 010018, China; Vegetable Research Center of Beijing Academy of Agriculture and Forestry Sciences, Beijing 100097, China;College of Animal Science and Medicine, Inner Mongolia Agricultural University, Hohhot 010018, China;Vegetable Research Center of Beijing Academy of Agriculture and Forestry Sciences, Beijing 100097, China;Vegetable Research Center of Beijing Academy of Agriculture and Forestry Sciences, Beijing 100097, China;Vegetable Research Center of Beijing Academy of Agriculture and Forestry Sciences, Beijing 100097, China;Vegetable Research Center of Beijing Academy of Agriculture and Forestry Sciences, Beijing 100097, China; Beijing Research Center for Agri-food Testing and Farmland Monitoring, Beijing 100097, China
Abstract:The environmental pollution by heavy metals such as mercury, cadmium and lead has become a worldwide public health hazard. To rapidly and inexpensively monitor environmental heavy metals is a prerequisite for minimizing human and animal exposure. The development of immunoassays to detect mercury ion residues has been a promising trend with the advantage of rapid and cheap operation. We reported the isolation and characterization of mercury-specific monoclonal antibodies. Because Hg2+ ions are too small to elicit an immune response, the metal was coupled to protein carrier (keyhole limpet, KLH) using a chelator (diethylenetriamine pentaacetic acid, DTPA). After the synthesis of antigen and characterization, monoclonal antibodies against mercury ions were generated by immunizing BALB/c mice with mercury conjugated antigen (Hg-DTPA-KLH). The stable hybridoma cell lines were produced by fusion of murine splenocytes and SP2/0 myeloma cells. The hybridoma cells were subcloned by the limiting dilution and screened by ELISA, two hybridoma cell lines producing stably specific monoclonal antibodies (MAbs) against mercury ions were obtained, named H2H5 and H1H8. The ascites fluid was produced in BABL/c mice by intraperitoneal injection of 1×107 H2H5 and H1H8 cells, respectively. The titers of ascites were all above 1:51 200. The isotyping of secrete antibodies from two hybridoma cell lines was IgG1, kappa type. These data laid a potency of establishing immunoassays methods of determining Hg2+ ion residues and had the realistic significance for improving the efficiency and quality of risk assessment.
Keywords:mercury  chelated antigen  monoclonal antibody  ELISA
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