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

被引:389
作者
Sawasaki, T
Ogasawara, T
Morishita, R
Endo, Y [1 ]
机构
[1] Ehime Univ, Dept Appl Chem, Fac Engn, Matsuyama, Ehime 7908577, Japan
[2] Ehime Univ, Venture Business lab, Matsuyama, Ehime 7908577, Japan
关键词
D O I
10.1073/pnas.232580399
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
We report a cell-free system for the high-through put 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.
引用
收藏
页码:14652 / 14657
页数:6
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