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梅毒螺旋体重组蛋白Tp1038的表达与鉴定

刘小军 蒋传好 曾铁兵 赵飞骏 余坚 吴移谋

医学信息Issue(14):266-267,2.
医学信息Issue(14):266-267,2.

梅毒螺旋体重组蛋白Tp1038的表达与鉴定

Expression and Identification of Recombinant Protein Tp1038 of Treponema Pallidum

刘小军 1蒋传好 2曾铁兵 3赵飞骏 3余坚 3吴移谋3

作者信息

  • 1. 南华大学附属第一医院血液科,湖南 衡阳421001
  • 2. 南华大学医学院病原生物学研究所,湖南 衡阳421001
  • 3. 南华大学医学院病原生物学研究所,湖南 衡阳421001
  • 折叠

摘要

Abstract

Objective To express and identify recombinant protein Tp1038 (rTp1038) of Treponema pal idum (Tp), providing a basis for further investigation of its significance in syphilis serodiagnosis. Methods PCR was used to amplify ful length of Tp1038 gene. The prokaryotic expression recombinant pET-28a (+)/Tp1038 was constructed and transformed into E.coli BL21 for expressing rTp1038. rTp1038 were purified with Ni-NTA af inity chromatography. SDS-PAGE was used to analyse expression form and purity of rTp1038. Western blot was performed to identify antigenicity of rTp1038. Results The prokaryotic recombinant pET-28a (+)/Tp1038 was constructed successful y and an approximate 20 KDa recombinant protein was expressed ef iciently in E.coli with dominant soluble form and more than 98% purity. Western blot indicated that purified proteins were able to be recognized special y by ant-His monoclonal antibody and pooled sera from syphilis patients. Conclusions The soluble recombinant Tp1038 are expressed ef iciently in E.coli and have good antigenicity and specifity.

关键词

梅毒螺旋体/Tp1038/重组抗原/抗原性

Key words

Treponema pal idum/Tp1038/Recombinant antigen/Antigenicity

引用本文复制引用

刘小军,蒋传好,曾铁兵,赵飞骏,余坚,吴移谋..梅毒螺旋体重组蛋白Tp1038的表达与鉴定[J].医学信息,2013,(14):266-267,2.

基金项目

国家自然科学基金(81273322);湖南省自然科学基金重点项目(11JJ2044);湖南省研究生培养创新项目 (81273322)

医学信息

1006-1959

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