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A cell-free protein synthesis system for high-throughput proteomics

机译:用于高通量蛋白质组学的无细胞蛋白质合成系统

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摘要

We report a cell-free system for the high-throughput synthesis and screening of gene products. The system, based on the eukaryotic translation apparatus of wheat seeds, has significant advantages over other commonly used cell-free expression systems. To maximize the yield and throughput of the system, we optimized the mRNA UTRs, designed an expression vector for large-scale protein production, and developed a new strategy to construct PCR-generated DNAs for high-throughput production of many proteins in parallel. The resulting system achieves high-yield expression and can maintain productive translation for 14 days. Additionally, in the integration of a PCR-directed system for template creation, at least 50 genes can be translated in parallel, yielding between 0.1 and 2.3 mg of protein by one person within 2 days. Assessment of correct protein folding by the products of this high-throughput protein-expression system were performed by enzymatic assays of kinases and by NMR spectroscopic analysis. The cell-free system, reported here, bypasses many of the time-consuming cloning steps of conventional expression systems and lends itself to a robotic automation for the high-throughput expression of proteins.
机译:我们报告了无细胞系统的高通量合成和基因产物的筛选。该系统基于小麦种子的真核翻译设备,与其他常用的无细胞表达系统相比具有明显的优势。为了最大程度地提高系统的产量和通量,我们优化了mRNA UTR,设计了用于大规模蛋白质生产的表达载体,并开发了一种新的策略来构建PCR生成的DNA,用于并行高通量生产许多蛋白质。生成的系统实现了高产量的表达,可以维持14天的高效翻译。此外,在集成了PCR指导的模板创建系统的过程中,至少50个基因可以并行翻译,一个人在2天内可产生0.1到2.3 mg的蛋白质。通过激酶的酶促测定和NMR光谱分析,评估了这种高通量蛋白质表达系统产品正确折叠的蛋白质。本文报道的无细胞系统绕过了传统表达系统许多耗时的克隆步骤,并使其自动实现了蛋白质高通量表达的机器人自动化。

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