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人β-干扰素的化学诱变:亚硫酸氢钠诱导突变体的构建、在大肠杆菌中的表达及生物学活性

Chemical mutagenesis of human interferon-beta: construction, expression in E. coli, and biological activity of sodium bisulfite-induced mutations.

作者信息

Stewart A G, Adair J R, Catlin G, Hynes C, Hall J, Davies J, Dawson K, Porter A G

出版信息

DNA. 1987 Apr;6(2):119-28. doi: 10.1089/dna.1987.6.119.

Abstract

A series of modified human interferon-beta (IFN-beta) genes was produced by sodium bisulfite treatment of the IFN-beta gene cloned in M13. A library of mutated sequences was generated from which subgenomic fragments containing one or a small number of coding alterations were isolated and substituted into the IFN-beta gene in an E. coli expression vector. A number of modified genes and their expression products were evaluated. In several instances levels of expression and biological activity profiles are altered compared to the parental gene product. A number of key amino acids can be identified, whose substitutions have marked effects on biological activity of IFN-beta.

摘要

通过亚硫酸氢钠处理克隆于M13的干扰素-β(IFN-β)基因,产生了一系列修饰的人IFN-β基因。由此生成了一个突变序列文库,从中分离出含有一个或少量编码改变的亚基因组片段,并将其替换到大肠杆菌表达载体中的IFN-β基因中。对多个修饰基因及其表达产物进行了评估。在一些情况下,与亲本基因产物相比,表达水平和生物学活性谱发生了改变。可以鉴定出一些关键氨基酸,其取代对IFN-β的生物学活性有显著影响。

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