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首页|期刊导航|中国肿瘤生物治疗杂志|ENO1蛋白及其相关活性位点缺失突变蛋白在昆虫杆状病毒表达系统中的表达与鉴定

ENO1蛋白及其相关活性位点缺失突变蛋白在昆虫杆状病毒表达系统中的表达与鉴定

代鹏钰 杨蕊 章婷婷 马昕芸 刘会玲

中国肿瘤生物治疗杂志2024,Vol.31Issue(7):669-674,6.
中国肿瘤生物治疗杂志2024,Vol.31Issue(7):669-674,6.DOI:10.3872/j.issn.1007-385x.2024.07.004

ENO1蛋白及其相关活性位点缺失突变蛋白在昆虫杆状病毒表达系统中的表达与鉴定

Expression and characterization of ENO1 protein and its associated active site deletion mutant proteins in a baculovirus expression vector system

代鹏钰 1杨蕊 1章婷婷 1马昕芸 1刘会玲2

作者信息

  • 1. 甘肃中医药大学 第一临床医学院 妇科二,甘肃 兰州 730000
  • 2. 甘肃中医药大学 甘肃省人民医院妇科二,甘肃 兰州 730000
  • 折叠

摘要

Abstract

Objective:To express the glycolytic enzyme alpha-enolase(ENO1)and its three enzyme active site deletion mutant ENO1 proteins(ENO-M1,pFastBac-M2,ENO1-M3)using a baculovirus expression vector system(insect BEVS),laying the groundwork for the subsequent study of metabolic therapy for cervical cancers.Methods:Molecule cloning was used to insert optimized ENO1 gene sequence into the pFastBacTM1 vector to obtain the recombinant plasmid pFastBac-ENO1 with target genes.Three active sites essential for ENO1's glycolytic function were deleted,and the corresponding optimized sequences were inserted into the pFastBacTM1 vector to generate the recombinant plasmids with three active site deletion,namely pFastBac-M1,pFastBac-M2 and pFastBac-M3.Recombinant baculoviruses rBV-ENO1,rBV-M1,rBV-M2 and rBV-M3 were subsequently obtained through transposition and transfection.The expression and specificity of the target proteins were examined using WB assay.Results:Recombinant bacilli rBacmid-ENO1,rBacmid-M1,rBacmid-M2 and rBacmid-M3 were successfully amplified,obtaining a gene fragment of about 2 000 bp in size,which was consistent with the expected size.The insect BEVS could express the ENO1 protein and its recombinant proteins(ENO1-M1,ENO1-M2,ENO1-M3)with three enzyme active site deletions,each with a molecular weight of approximately 52 000,as expected.WB analysis confirmed that these proteins reacted with the specific His-tag antibody.Conclusion:The insect BEV successfully expresses the target protein and its proteins with enzyme active site deletions,namely ENO1-M1,ENO1-M2 and ENO1-M3.This protein's reactivity establishes the foundation for subsequent determination of the affinity of these proteins,and ENO1 monoclonal antibody.

关键词

α-烯醇化酶/昆虫杆状病毒表达系统/蛋白表达/酶活性位点缺失

Key words

enolase 1(ENO1)/baculovirus expression vector system(BEVS)/protein expression/loss of enzyme activity sites

分类

生物科学

引用本文复制引用

代鹏钰,杨蕊,章婷婷,马昕芸,刘会玲..ENO1蛋白及其相关活性位点缺失突变蛋白在昆虫杆状病毒表达系统中的表达与鉴定[J].中国肿瘤生物治疗杂志,2024,31(7):669-674,6.

基金项目

国家自然科学基金(No.82260557) (No.82260557)

中国肿瘤生物治疗杂志

OA北大核心CSTPCD

1007-385X

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