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在无细胞PURE系统中,蛋白质合成产量提高了72倍。

Protein synthesis yield increased 72 times in the cell-free PURE system.

作者信息

Jackson Kirsten, Kanamori Takashi, Ueda Takuya, Fan Z Hugh

机构信息

J. Crayton Pruitt Family Department of Biomedical Engineering, University of Florida, P.O. Box 116131, Gainesville, FL 32611, USA.

出版信息

Integr Biol (Camb). 2014 Aug;6(8):781-8. doi: 10.1039/c4ib00088a.

DOI:10.1039/c4ib00088a
PMID:25008400
Abstract

Compared to cell-based protein expression, cell-free protein synthesis (CFPS) offers several advantages including a greater control over system additives. This control is further enhanced with a CFPS system called the Protein synthesis Using Recombinant Elements (PURE) system, which consists of 108 purified transcriptional and translational elements. With the PURE system, all elements are known, nuclease and protease activities are reduced, and the concentration of each element can be optimized for maximal protein expression. However, protein expression yield with this system is relatively low due to the consumption of nutrients and energy molecules as well as the accumulation of inhibitory byproducts in the batch format. To enhance protein expression with the PURE system, we developed a feeding solution that was optimized using a miniaturized fluid array device (μFAD) in a continuous-exchange cell-free (CECF) format. The device enabled (1) continuous supply of energy/nutrient molecules from the feeding solution to the reaction solution where protein synthesis occurred, and (2) simultaneous removal of inhibitory expression byproducts from the reaction solution to the feeding solution. Consequently, the synthesis yield of green fluorescent protein (GFP) increased 72.5-fold in comparison with the same reaction in the conventional batch format.

摘要

与基于细胞的蛋白质表达相比,无细胞蛋白质合成(CFPS)具有多个优点,包括对系统添加剂有更强的控制能力。一种名为“利用重组元件进行蛋白质合成(PURE)系统”的CFPS系统进一步增强了这种控制能力,该系统由108种纯化的转录和翻译元件组成。使用PURE系统时,所有元件都是已知的,核酸酶和蛋白酶活性降低,并且可以对每个元件的浓度进行优化以实现最大程度的蛋白质表达。然而,由于营养物质和能量分子的消耗以及批式反应中抑制性副产物的积累,该系统的蛋白质表达产量相对较低。为了提高PURE系统的蛋白质表达水平,我们开发了一种补料溶液,该溶液使用微型流体阵列装置(μFAD)以连续交换无细胞(CECF)形式进行了优化。该装置能够(1)将能量/营养分子从补料溶液连续供应到发生蛋白质合成的反应溶液中,以及(2)将抑制性表达副产物从反应溶液中同时去除到补料溶液中。因此,与传统批式反应相比,绿色荧光蛋白(GFP)的合成产量提高了72.5倍。

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