Tanaka Yo, Shimizu Yoshihiro
Laboratory for Integrated Biodevice, Quantitative Biology Center (QBiC), RIKEN.
Anal Sci. 2015;31(2):67-71. doi: 10.2116/analsci.31.67.
Recently, a cell-free protein synthesis system reconstituted solely from essential elements of the Escherichia coli translation system, termed protein synthesis using recombinant elements (PURE), has been widely used in synthetic biology to analyze fundamental life systems. Here, the system was integrated on a glass microchip system to construct a simple protein synthesis system. GFP template DNAs were immobilized on Sepharose microbeads by streptavidin-biotin binding. The beads were introduced into a Y-shaped microchannel in a glass microchip with a 10-μm height dam structure, and a PURE system reaction mixture was flowed through the microchannel. The recovered solutions had a higher fluorescent intensity than that of the reaction mixture before its introduction into the microchannel, thus verifying that GFP synthesis had been achieved. The microchip with DNA immobilized microbeads is reusable. This is advantageous over a conventional in vitro protein synthesis protocol requiring the preparation and addition of template DNA or mRNA into the reaction mixtures in aspect of simpleness and rapidness.
最近,一种仅由大肠杆菌翻译系统的基本元件重构的无细胞蛋白质合成系统,即使用重组元件的蛋白质合成(PURE)系统,已在合成生物学中广泛用于分析基本生命系统。在此,该系统被整合到玻璃微芯片系统上,以构建一个简单的蛋白质合成系统。绿色荧光蛋白(GFP)模板DNA通过链霉亲和素-生物素结合固定在琼脂糖微珠上。将这些微珠引入具有10μm高坝结构的玻璃微芯片中的Y形微通道中,然后使PURE系统反应混合物流过该微通道。回收的溶液的荧光强度高于其引入微通道之前的反应混合物,从而证实已实现了GFP的合成。固定有DNA的微珠的微芯片可重复使用。在简单性和快速性方面,这比传统的体外蛋白质合成方案更具优势,传统方案需要在反应混合物中制备并添加模板DNA或mRNA。