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[人白细胞介素-4合成基因在大肠杆菌细胞中的表达。生物活性蛋白的制备]

[Expression of a synthetic gene for human interleukin-4 in E. coli cells. Preparation of a biologically active protein].

作者信息

Batchikova N V, Kulagina M A, Lutsenko S V, Smirnov V A, Kanevskiĭ V Iu, Riazanova L A, Nazimov I V, Sonina N V, Siniagina E A, Azhaev A V

出版信息

Bioorg Khim. 1992 May;18(5):660-70.

PMID:1417993
Abstract

Expression E. coli plasmid were constructed in which the human interleukin-4 (hIL4) synthetic gene is controlled by tac promoter. The expression level of the gene depends on the distance between RBS and the initial codon ATG, with the maximal production in case of the nine base pair distance. The recombinant protein, accumulated in the inclusion bodies, was solubilized, renaturated, and purified to homogeneous, biologically active preparation, the yield being 2 mg/g wet cells.

摘要

构建了大肠杆菌表达质粒,其中人白细胞介素 -4(hIL4)合成基因由tac启动子控制。该基因的表达水平取决于核糖体结合位点(RBS)与起始密码子ATG之间的距离,当距离为9个碱基对时产量最高。积聚在包涵体中的重组蛋白经溶解、复性和纯化,得到均一的、具有生物活性的制剂,产量为每克湿细胞2毫克。

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