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pCold-GST vector: A novel cold-shock vector containing GST tag for soluble protein production

机译:pCold-GST载体:含有GST标签的新型冷休克载体,用于可溶性蛋白生产

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摘要

The production of recombinant protein in Escherichia coli is often hampered by low expression levels and low solubility. A variety of methodologies have been developed including protein production at low temperature, and fusion protein expression using soluble protein tags. Here, we present the novel cold-shock vector pCold-GST for high-level expression of soluble proteins in E coli. This vector is a modified pCold I cold-shock vector that includes the glutathione S-transferase (GST) tag. The pCold-GST expression system developed was applied to 10 proteins that could not be expressed using conventional E. coli expression methodologies, and nine of these proteins were successfully obtained in the soluble fraction. The expression and purification of two unstable protein fragments were also demonstrated by employing a C-terminal hexa-histidine tag for purification purposes. The purified proteins were amenable to NMR analyses. These data suggest that the pCold-GST expression system can be utilized to improve the expression and purification of various proteins. (C) 2008 Elsevier Inc. All rights reserved.
机译:低表达水平和低溶解度通常会阻碍大肠杆菌中重组蛋白的产生。已经开发了多种方法,包括在低温下生产蛋白质,以及使用可溶性蛋白质标签表达融合蛋白。在这里,我们提出了新型的冷休克载体pCold-GST,用于大肠杆菌中可溶性蛋白的高水平表达。该载体是修饰的pCold I冷休克载体,包含谷胱甘肽S-转移酶(GST)标签。开发的pCold-GST表达系统应用于使用常规大肠杆菌表达方法无法表达的10种蛋白质,并且在可溶性级分中成功获得了其中的9种蛋白质。还通过将C-末端六组氨酸标签用于纯化目的来证明两个不稳定蛋白片段的表达和纯化。纯化的蛋白质适合于NMR分析。这些数据表明,pCold-GST表达系统可用于改善各种蛋白质的表达和纯化。 (C)2008 Elsevier Inc.保留所有权利。

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