吉林大学学报(医学版)

• 基础研究 • 上一篇    下一篇

野生型和失活型PAK1基因自我抑制域的GST标签真核表达载体的构建及表达

刘彤,李丹妮*,李洋,李丰   

  1. (中国医科大学基础医学院细胞生物学教研室 教育部医学细胞生物学重点实验室,辽宁 沈阳 110001)
  • 收稿日期:2012-11-16 出版日期:2014-01-28 发布日期:2014-01-28
  • 通讯作者: 李 丰 E-mail:(Tel:024-23261056,E-mail:fli@mail.cmu.edu.cn)
  • 作者简介:刘 彤(1980-),女,辽宁省沈阳市人,副教授,医学博士,主要从事肿瘤与信号转导研究。
  • 基金资助:

    国家自然科学基金资助课题(31171360,81302238);辽宁省教育厅科学研究一般项目资助课题(L2013304)

Construction and expression of wild type and  inactive type of GST-tagged eukaryotic expression vectors of PAK1 gene autoinhibitory domain

LIU Tong,LI Dan-ni*,LI Yang,LI Feng   

  1. (Department of Cell Biology,School of Basic Medical Sciences,Key Laboratory of Medical Cell Biology,Ministry of Education,China Medical University,Shenyang 110001,China)
  • Received:2012-11-16 Online:2014-01-28 Published:2014-01-28

摘要:

目的:构建不同活性的人p21活化激酶1(hPAK1)自我抑制域(AID)谷胱甘肽(GST)标签真核表达载体并鉴定其融合蛋白表达,以探讨PAK1 AID的功能及肿瘤治疗的靶向意义。方法:以pcDNA3.1HisC-PAK1全长质粒为模板,利用PCR扩增野生型(WT)PAK1 AID片段,再以此片段为模板采用大引物法扩增其突变体L107F片段,双酶切克隆至GST融合的真核表达载体pEBG。将质粒转染至工具细胞HEK293中,并经免疫印迹鉴定GST融合蛋白的表达。结果:PCR扩增出约200 bp大小的野生型和失活型PAK1 AID片段,双酶切得到与预期大小相符的载体与PAK1 AID片段,野生型与失活型pEBG-PAK1在工具细胞HEK293中表达,蛋白的相对分子质量均为33 000。结论:成功构建野生型和失活型PAK1基因 AID的GST标签真核表达载体,并表达出不同活性的GST-PAK1 AID的融合蛋白。

关键词: p21活化激酶1, 自我抑制域, 失活型(L107F), 真核表达, GST标签

Abstract:

To construct the GST-tagged eukaryotic expression vectors of human p21-activated kinase 1(hPAK1) autoinhibitory domain(AID) with different activities and identify the expressions of their recombinant proteins,and to explore the function of PAK1 AID and molecular targeting role in tumor therapy.Methods The pcDNA3.1HisC-PAK1 full length plasmid was used as template,and the fragment of wild PAK1 AID was amplified with PCR,and the fragment of PAK1 L107F was amplified with long primer mutant method.The PCR fragments were double-digested and cloned into pEBG.The wild and inactive types of pEBG-PAK1 were transfected into HEK293 cells and their expressions were identified by Western blotting.Results The wild and in active PAK1 AID  fragments with 200 bp  were obtained by PCR.5 000 bp vector band and 200 bp PAK1 AID band were obtained by double-digestion.The wild and inactive types of  pEBG-PAK1  were expressed in HEK293 cells,and the molecular weight of the protein was 33 000.Conclusion The wild and inactive types of PAK1 AID  eukaryotic expression vectors are successfully constructed.The expressions of wild and inactive  types of PAK1 AID proteins  are identified.

Key words: p21-activated kinase 1, autoinhibitory domain, inactive type(L107F), eukaryotic expression, GST-tag

中图分类号: 

  • R730.23