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CONSTRUCTION, EXPRESSION AND BIOLOGICAL ASSESSMENT OF BPI_(23)-Fcγ1 RECOMBINANT PROTEIN PROKARYOTIC EXPRESSION VECTOR 被引量:7
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作者 安云庆 管远志 +1 位作者 柯岩 杨贵贞 《Chinese Medical Sciences Journal》 CAS CSCD 2002年第3期140-147,共8页
关键词 pBV BPI600 Fcγ1700 recombinant expression vector BPI23 Fcγ1 recombinant protein Objective. To construct pBV BPI600 Fcγ1700 recombinant expression vector to transform it into Escherichia coli DH5α and to induce the expression of BPI2
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Expression and purification of recombinant human hemangiopoietin in Escherichia coli
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作者 Ren Qian Ma Fengxia Chen Zhong Lu Shihong Han Zhibo Liu Yongjun Xu Bin Zhang Xiangyu Han Zhongchao 《Journal of Medical Colleges of PLA(China)》 CAS 2008年第3期148-153,共6页
Objective:To express the soluble recombinant hemangiopoietin protein in E.coli BL21(DE3).Methods:Using human fetal live cDNA as a template,a partial cDNA fragment of HAPO coding N-terminal region was subcloned into pl... Objective:To express the soluble recombinant hemangiopoietin protein in E.coli BL21(DE3).Methods:Using human fetal live cDNA as a template,a partial cDNA fragment of HAPO coding N-terminal region was subcloned into plasmids pTrc99,pQE60 and pET32c to construct different recombinant prokaryotic expression systems.After selecting,the soluble rhHAPO fusion protein was expressed stably in E.coli BL21(DE3) by vector pET32c-HAPO and further isolated by nickelnitrilotriacetic acid(NTA) affinity chromatography.After cleavage with enterokinase,the rhHAPO protein was applied to Fast Flow SP sepharose column.Results:The rhHAPO protein had a purity of more than 95% and a good bioactivity based on the cell adhesion assay in ECV304 cells.Conclusion:We have established a protein engineering system to produce rhHAPO which may provide the possibility for clinical application. 展开更多
关键词 ENTEROKINASE Escherichia coli Fusion protein Hemangiopoietin PURIFICATION recombinant protein expression
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