摘要
利用双Tac启动子和改造后的人白细胞介素2(IL-2)cDNA,提高了IL-2在大肠杆菌(E.Coli)中的表达水平,并经包涵体制备、分子重新折叠及分子筛层析等技术,对表达的IL-2进行了提取、活性恢复与纯化,纯度可达95%。本工作为用基因工程方法生产人IL-2积累了经验。
Human interleukin 2 (IL-2) has been highly expressed in E. colt by inserting IL-2 cDNA with deletion in 3' non-coding region down to double Tao promoters. The ex pressed 1L-2 forming inclusion body in bacteria cells was isolated, refolded, and subject to sephadex G-75 chromatography. As a result, the IL-2 was highly purified to 95% with the biological activity recovered. The work enriched the experience of IL-2 production by incor porating methods of genetic engineering.
出处
《同济医科大学学报》
CAS
CSCD
北大核心
1994年第1期15-18,共4页
Acta Universitatis Medicinae Tongji
关键词
基因表达
大肠杆菌
白细胞介素2
gene expression,E.coli,lymphocyte,interleukin 2,isolation and purification,inclusion body