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High-throughput, genome-scale protein production method based on the wheat germ cell-free expression system

机译:基于无小麦生殖细胞表达系统的高通量,基因组规模的蛋白质生产方法

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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.
机译:当前的无细胞蛋白质表达系统能够快速,准确地合成蛋白质。然而,由于其随时间的不稳定,收率很低。基于大肠杆菌的系统并不总是足以表达真核蛋白。本报告回顾了基于从真核生物,小麦胚制备的无细胞系统的高通量蛋白质生产方法。我们首先证明了该提取物的制备方法,该方法表现出高度的稳定性和活性。为了最大程度地提高翻译产量和吞吐量,我们解决并解决以下问题:(1)优化ORF侧翼区域; (2)基于PCR的DNA的产生以产生mRNA; (3)用于大规模蛋白质生产的表达载体; (4)不需要膜的翻译反应。这些基本过程与机器人自动化的结合导致了高通量的蛋白质合成。

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