Chen Xinjie, Lu Yuan
Key Laboratory of Industrial Biocatalysis, Ministry of Education, Department of Chemical Engineering, Tsinghua University, Beijing, China.
Front Bioeng Biotechnol. 2021 May 18;9:670341. doi: 10.3389/fbioe.2021.670341. eCollection 2021.
Cell-free gene expression systems with linear DNA expression templates (LDETs) have been widely applied in artificial cells, biochips, and high-throughput screening. However, due to the degradation caused by native nucleases in cell extracts, the transcription with linear DNA templates is weak, thereby resulting in low protein expression level, which greatly limits the development of cell-free systems using linear DNA templates. In this study, the protective sequences for stabilizing linear DNA and the transcribed mRNAs were rationally designed according to nucleases' action mechanism, whose effectiveness was evaluated through computer simulation and cell-free gene expression. The cell-free experiment results indicated that, with the combined protection of designed sequence and GamS protein, the protein expression of LDET-based cell-free systems could reach the same level as plasmid-based cell-free systems. This study would potentially promote the development of the LDET-based cell-free gene expression system for broader applications.
具有线性DNA表达模板(LDETs)的无细胞基因表达系统已广泛应用于人工细胞、生物芯片和高通量筛选。然而,由于细胞提取物中天然核酸酶引起的降解,线性DNA模板的转录较弱,从而导致蛋白质表达水平较低,这极大地限制了使用线性DNA模板的无细胞系统的发展。在本研究中,根据核酸酶的作用机制合理设计了用于稳定线性DNA和转录mRNA的保护序列,并通过计算机模拟和无细胞基因表达对其有效性进行了评估。无细胞实验结果表明,在设计序列和GamS蛋白的联合保护下,基于LDET的无细胞系统的蛋白质表达可以达到与基于质粒的无细胞系统相同的水平。本研究可能会促进基于LDET的无细胞基因表达系统的发展,以实现更广泛的应用。