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华支睾吸虫3-磷酸甘油醛脱氢酶重组蛋白的纯化、酶学活性及免疫学研究
引用本文:张咏莉,吴德,余新炳. 华支睾吸虫3-磷酸甘油醛脱氢酶重组蛋白的纯化、酶学活性及免疫学研究[J]. 中国寄生虫学与寄生虫病杂志, 2005, 23(4): 231-235
作者姓名:张咏莉  吴德  余新炳
作者单位:1. 广东药学院基础学院生物教研室,广州,510224;中山大学基础医学院病原生物学部寄生虫教研室,广州,510089
2. 中山大学基础医学院病原生物学部寄生虫教研室,广州,510089
基金项目:广东省自然科学基金团队资助项目(No.20003026);“211”重点学科建设基金(No.98169);国家教育部博士点基金(博教No.93-186)
摘    要:目的体外制备华支睾吸虫3-磷酸甘油醛脱氢酶重组蛋白(CsGAPDH),分析其酶学活性及免疫学特性。方法常规表达重组质粒pGEX-4T-1-GAPDH,用谷胱甘肽-S-转移酶(GST)亲和纯化试剂盒纯化重组蛋白,经十二烷基磺酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE),用凝血酶和纯化柱酶切、纯化的CsGAPDH免疫BALB/c小鼠,制备抗血清。ELISA检测抗IgG抗体滴度,浓缩型S-P免疫组化3步法检测CsGAPDH抗原在免疫小鼠体内的分布和表达。蛋白质印迹法(Western blotting)鉴定其抗血清的特异性。建立酶反应体系测定重组蛋白CsGAPDH的酶催化活性。结果纯化蛋白样品呈单一条带。免疫动物获取CsGAPDH抗血清,在免疫过程中抗体滴度呈连续上升趋势。CsGAPDH抗原分布和表达于小鼠肌细胞膜部位。免疫小鼠血清具有抗CsGAPDH特异性抗体。重组蛋白CsGAPDH具有酶生理活性,其酶活力单位为2 872 U min-1.ml-1。结论制备的重组蛋白CsGAPD H具有较好的酶活性和免疫原性。

关 键 词:华支睾吸虫  3-磷酸甘油醛脱氢酶  蛋白质印迹法  免疫原性
文章编号:1000-7423(2005)-04-0231-05
收稿时间:2005-03-13
修稿时间:2005-03-13

Purification, Enzyme Activity and Immunology Study of Recombinant Protein Glyceraldehyde-3-phosphate Dehydrogenase of Clonorchis sinensis
ZHANG Yong-li,WU De,YU Xin-Bing. Purification, Enzyme Activity and Immunology Study of Recombinant Protein Glyceraldehyde-3-phosphate Dehydrogenase of Clonorchis sinensis[J]. Chinese Journal of Parasitology and Parasitic Diseases, 2005, 23(4): 231-235
Authors:ZHANG Yong-li  WU De  YU Xin-Bing
Affiliation:Department of Medical biology, Guangdong Pharmaceutical University, Guangzhou 510224, China.
Abstract:OBJECTIVE: To produce prokaryotic recombinant protein glyceraldehyde-3 phosphate dehydrogenase of Clonorchis sinensis (CsGAPDH), analyze its enzyme activity and immunological function. Methods The recombinant CsGAPDH was purified according to the protocol of GST-Bind kit and was digested with thrombin proteinase and eluted with wash buffer. The BALB/c mice were inoculated with the purified protein. The antisera collected from the mice were used to detect the titres of IgG antibodies by ELISA, and Western blotting was used to identify the specificity of the antisera with the purified CsGAPDH. S-P immunohistochemistry method was used to confirm the expression and distribution of CsGAPDH in adult Clonorchis sinensis with the polyclonal antibodies from immunized BALB/c mice. The CsGAPDH catalytic activity was evaluated employing the conventional substrate glyceraldehydes-3-phosphate (3-GAP). RESULTS: SDS-PAGE showed a single purified protein band. Gel scanning analysis revealed that the protein purity of CsGAPDH was 90%. ELISA analysis showed an increased IgG value. S-P immunohistochemistry analysis demonstrated that the recombinant plasmid pGEX-4T-1 GAPDH expressed and distributed in muscle cell membrane of immune mice. Western blotting result suggested that CsGAPDH protein contained essential epitopes with high antigenic activities. This protein CsGAPDH could catalyzed 3-GAP with enzymatic active unit of 2872 U min(-1) ml(-1). CONCLUSION: The recombinant protein CsGAPDH shows a proper enzymatic activity and immunogenicity.
Keywords:Clonorchis sinensis  Glyceraldehyde-3-phosphate dehydrogenase (GAPDH)  Western blotting  Immunogenicity
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