首页 | 本学科首页   官方微博 | 高级检索  
检索        

幽门螺杆菌尿素酶A、过氧化氢酶的表达及纯化
引用本文:廖文俊,陈湖,朱森林,陈洁,陈为,胡品津.幽门螺杆菌尿素酶A、过氧化氢酶的表达及纯化[J].中国免疫学杂志,2001,17(7):348-350.
作者姓名:廖文俊  陈湖  朱森林  陈洁  陈为  胡品津
作者单位:1. 第四军医大学附属西京医院皮肤科,
2. 中山医科大学附属第一医院消化内科,
基金项目:卫生部临床学科重点项目(No.97040226)、广东省科技计划重点攻关项目(No.99No4802G)和广东省自然科学基金课题(No.990077)
摘    要:目的:探讨重组尿素酶A亚单位(UreA)、过氧化氢酶(KatA)疫苗在防治婴门螺杆菌(HP)感染中的作用。方法:构建表达UreA、KatA的重组质粒,用IPTG诱导表达融合蛋白,并进行SDS-PAGE凝胶电泳及Western blot分析,Bulk GST Purification Module试剂盒纯化UreA和KatA。结果:构建的重组质粒能表达GST-UreA和GST-KatA合蛋白,表达量占细胞总蛋白量的35%和19%,并能与抗GST 发生特异性反应。纯化的UreA、KatA的纯度达95%以上。结论:该工作为进一步的动物免疫实验奠定了基础,该重组疫苗有望在HP感染及其相关疾病的防治中发挥积极作用。

关 键 词:幽门螺杆菌  疫苗  尿素酶A  过氧化氢酶
文章编号:1000-484X(2001)07-0348-03

Expression and purification of Helicobacter pylori urease A subunit and catalase
LIAO Wen Jun,CHEN Min Hu,ZHU Sen Lin et al.Expression and purification of Helicobacter pylori urease A subunit and catalase[J].Chinese Journal of Immunology,2001,17(7):348-350.
Authors:LIAO Wen Jun  CHEN Min Hu  ZHU Sen Lin
Institution:LIAO Wen Jun,CHEN Min Hu,ZHU Sen Lin et al Department of Gastroenterology,The First Affiliated Hospital,Sun Yat Sen University of Medical Sciences,Guangzhou 510080
Abstract:Objective:Investigated the effect of recombinant urease A subunit and catalase vaccines on protection against Helicobacter pylori (HP) infection Methods:Recombinant plasmids expressing UreA or KatA were constructed Expression was induced with IPTG,analyzed by SDS PAGE and Western blot UreA and KatA were purified with Bulk GST purification module Results:The recombinant plasmids could express GST UreA and GST KatA fusion proteins,which accounted for 35% and 19% of total bacteria proteins respectively,and could specially react with antibody against GST The purity of the purified UreA and KatA was over 95% Conclusion:The work laid a foundation for further studies of HP vaccine The recombinant vaccines may play an important role in preventing and treating HP infection and related diseases
Keywords:Helicobacter pylori  Vaccine  KatA  Urease
本文献已被 CNKI 维普 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号