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SARS病毒核衣壳蛋白、膜蛋白在大肠杆菌中的高效表达和纯化
引用本文:易艳萍,李楚芳,石玉岭,李林海,李平,黄维,王升启,马清钧,曹诚.SARS病毒核衣壳蛋白、膜蛋白在大肠杆菌中的高效表达和纯化[J].生物工程学报,2003,19(4):392-396.
作者姓名:易艳萍  李楚芳  石玉岭  李林海  李平  黄维  王升启  马清钧  曹诚
作者单位:1. 军事医学科学院生物工程研究所,北京,100850
2. 广州军区总医院检验科,广州,510010
3. 军事医学科学院放射医学研究所,北京,100850
摘    要:通过反转录PCR获得了SARS冠状病毒核衣壳蛋白(N)和膜蛋白(M)基因,其序列分析结果与加拿大多伦多株完全一致。将M基因和N基因克隆到大肠杆菌表达载体pET22b和pBV222上,并在大肠杆菌中以包涵体及可溶形式获得高效表达。通过离子交换、金属螯合层析纯化获得电泳纯制品。所获得的核衣壳蛋白具有良好的抗原性,可用于抗SARS抗体检测及亚单位疫苗研究。

关 键 词:SARS病毒    核衣壳蛋白    膜蛋白    表达
文章编号:1000-3061(2003)04-0392-05
修稿时间:2003年5月22日

Over-expression in Escherichia coli and Purification of Nucleocaspid and Membrane Protein of SARS Coronavirus
YI Yan-Ping,LI Chu-Fang,SHI Yu-Ling,LI Lin-Hai,LI Ping,HUANG Wei,WANG Sheng-Qi,MA Qing-Jun,CAO Cheng.Over-expression in Escherichia coli and Purification of Nucleocaspid and Membrane Protein of SARS Coronavirus[J].Chinese Journal of Biotechnology,2003,19(4):392-396.
Authors:YI Yan-Ping  LI Chu-Fang  SHI Yu-Ling  LI Lin-Hai  LI Ping  HUANG Wei  WANG Sheng-Qi  MA Qing-Jun  CAO Cheng
Institution:Beijing Institute of Biotechnology, Beijing 100850, China.
Abstract:Genes encoding nucleocaspid (N) and membrane(M)protein of SARS coronavirus were obtained by RT-PCR and were cloned into expression vector pET22b and pBV222. DNA sequencing showed that the genes cloned from a patient in Beijing were identical to the gene sequences from reported Toronto strain. The genes were over-expressed in E.coli either as inclusion body or as soluble form. The recombinant proteins were purified by ion-exchange, or ion-exchange followed by metal chelate affinity chromatography. The recombinant N protein was demonstrated highly antigenic and could be employed as antigen to detect SARS antibodies in ELISA system for SARS diagnosis.
Keywords:SARS coronavirus  nucleocaspid protein  membrane protein  expression  
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