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一种新型的无细胞蛋白质合成系统。

A novel cell-free protein synthesis system.

作者信息

Sitaraman Kalavathy, Esposito Dominic, Klarmann George, Le Grice Stuart F, Hartley James L, Chatterjee Deb K

机构信息

SAIC-National Cancer Institute at Frederick, 1050 Boyles Street, Building 327, Frederick, MD 21702-1201, USA.

出版信息

J Biotechnol. 2004 Jun 10;110(3):257-63. doi: 10.1016/j.jbiotec.2004.02.014.

Abstract

An efficient cell-free protein synthesis system has been developed using a novel energy-regenerating source. Using the new energy source, 3-phosphoglycerate (3-PGA), protein synthesis continues beyond 2 h. In contrast, the reaction rate slowed down considerably within 30-45 min using a conventional energy source, phosphoenol pyruvate (PEP) under identical reaction conditions. This improvement results in the production of twice the amount of protein obtained with PEP as an energy source. We have also shown that Gam protein of phage lambda, an inhibitor of RecBCD (ExoV), protects linear PCR DNA templates from degradation in vitro. Furthermore, addition of purified Gam protein in extracts of Escherichia coli BL21 improves protein synthesis from PCR templates to a level comparable to plasmid DNA template. Therefore, combination of these improvements should be amenable to rapid expression of proteins in a high-throughput manner for proteomics and structural genomics applications.

摘要

利用一种新型能量再生源开发了一种高效的无细胞蛋白质合成系统。使用新的能量源3-磷酸甘油酸(3-PGA),蛋白质合成可持续超过2小时。相比之下,在相同反应条件下,使用传统能量源磷酸烯醇丙酮酸(PEP)时,反应速率在30-45分钟内显著减慢。这种改进使得以PEP作为能量源时获得的蛋白质产量提高了一倍。我们还表明,噬菌体λ的Gam蛋白是RecBCD(ExoV)的抑制剂,可在体外保护线性PCR DNA模板不被降解。此外,在大肠杆菌BL21提取物中添加纯化的Gam蛋白可将PCR模板的蛋白质合成提高到与质粒DNA模板相当的水平。因此,这些改进措施的结合应适合以高通量方式快速表达蛋白质,用于蛋白质组学和结构基因组学应用。

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