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融合蛋白CBD SPA“Z”基因的构建、表达与活性鉴定

朱文杰 马军 张妍 金坚

生物加工过程Issue(3):52-57,6.
生物加工过程Issue(3):52-57,6.DOI:10.3969/j.issn.1672-3678.2014.03.010

融合蛋白CBD SPA“Z”基因的构建、表达与活性鉴定

Construction,expression,and biological assay of fusion protein CBD-SPA Z

朱文杰 1马军 2张妍 2金坚1

作者信息

  • 1. 江南大学 药学院 无锡 214122
  • 2. 江南大学 生物工程学院教育部工业生物技术重点实验室,无锡 214122
  • 折叠

摘要

Abstract

To solve the problems of staphylococcal protein A(SPA) application,recombining the fusion protein of cellulose binding domain(CBD) with Z peptide of SPA,introducing a cysteine at the C-terminal of Z peptide, and construction and expression of immune affinity material were investigated�Prokaryotic expression vector pET35b(+)-Z-Cys was constructed by using the genetic engineering to clone the Z gene of pEZZ18 plasmid and inserted into the pET35b(+) plasmid with CBD gene,thus obtaining the fusion protein CBD-protein Z by IPTG�The plasmid pET35b(+)-Z-Cys was correctly expressed in E�coli BL21 and the fusion protein retained the bio-functional effects of Z peptide and CBD�CBD could bind to cellulose and Z peptide bind to immunoglobulin G( IgG) of many mammalians,via Fc region of IgG�

关键词

纤维素结合结构域/免疫亲和层析/金黄色葡萄球菌蛋白A/Z结构域/IgG纯化

Key words

cellulose binding domain/immunoaffinity chromatography/staphylococcal protein A/Z peptide/purification of IgG

分类

生物科学

引用本文复制引用

朱文杰,马军,张妍,金坚..融合蛋白CBD SPA“Z”基因的构建、表达与活性鉴定[J].生物加工过程,2014,(3):52-57,6.

基金项目

国家大学生创新训练计划 ()

生物加工过程

OACSTPCD

1672-3678

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