Endo Yaeta, Sawasaki Tatsuya
Cell-Free Science and Technology Research Center, and the Venture Business Laboratory, Ehime University, Matsuyama 790-8577, Japan.
J Struct Funct Genomics. 2004;5(1-2):45-57. doi: 10.1023/B:JSFG.0000029208.83739.49.
Current cell-free protein expression systems are capable of synthesizing proteins with high speed and accuracy; however, the yields are low due to their instability over time. Escherichia coli based systems are not always sufficient for expression of eukaryotic proteins. This report reviews a high-throughput protein production method based on the cell-free system prepared from eukaryote, wheat embryos. We first demonstrate a method for preparation of this extract that exhibited a high degree of stability and activity. To maximize translation yield and throughput, we address and resolve the following issues: (1) optimization of the ORF flanking regions; (2) PCR-based generation of DNA for mRNA production; (3) expression vectors for large-scale protein production; and (4) a translation reaction that does not require a membrane. The combination of these elemental processes with robotic automation resulted in high-throughput protein synthesis.
目前的无细胞蛋白质表达系统能够高速且准确地合成蛋白质;然而,由于其随时间的不稳定性,产量较低。基于大肠杆菌的系统对于真核蛋白质的表达并不总是足够的。本报告综述了一种基于从真核生物小麦胚制备的无细胞系统的高通量蛋白质生产方法。我们首先展示了一种制备该提取物的方法,该提取物表现出高度的稳定性和活性。为了使翻译产量和通量最大化,我们提出并解决了以下问题:(1)开放阅读框侧翼区域的优化;(2)基于PCR产生用于mRNA生产的DNA;(3)用于大规模蛋白质生产的表达载体;以及(4)不需要膜的翻译反应。这些基本过程与机器人自动化相结合,实现了高通量蛋白质合成。