Center for Molecular Recognition and Biosensing, Shanghai Engineering Research Center of Organ Repair, School of Life Sciences, Shanghai University, Shanghai 200444, P. R. China.
Department of Clinical Laboratory Medicine, Shanghai Tenth People's Hospital of Tongji University, Shanghai 200072, P. R. China.
ACS Synth Biol. 2023 Jun 16;12(6):1657-1666. doi: 10.1021/acssynbio.3c00003. Epub 2023 May 17.
Synthetic biological systems have been utilized to develop a wide range of genetic circuits and components that enhance the performance of biosensing systems. Among them, cell-free systems are emerging as important platforms for synthetic biology applications. Genetic circuits play an essential role in cell-free systems, mainly consisting of sensing modules, regulation modules, and signal output modules. Currently, fluorescent proteins and aptamers are commonly used as signal outputs. However, these signal output modes cannot simultaneously achieve faster signal output, more accurate and reliable performance, and signal amplification. Ribozyme is a highly structured and catalytic RNA molecule that can specifically recognize and cut specific substrate sequences. Here, by adopting ribozyme as the signal output, we developed a cell-free biosensing genetic circuit coupled with the ribozyme cleavage reaction, enabling rapid and sensitive detection of small molecules. More importantly, we have also successfully constructed a 3D-printed sensor array and thereby achieved high-throughput analysis of an inhibitory drug. Furthermore, our method will help expand the application range of ribozyme in the field of synthetic biology and also optimize the signal output system of cell-free biosensing, thus promoting the development of cell-free synthetic biology in biomedical research, clinical diagnosis, environmental monitoring, and food inspection.
合成生物学系统已被用于开发广泛的遗传电路和组件,以提高生物传感系统的性能。其中,无细胞系统作为合成生物学应用的重要平台正在兴起。遗传电路在无细胞系统中起着至关重要的作用,主要由传感模块、调节模块和信号输出模块组成。目前,荧光蛋白和适体通常被用作信号输出。然而,这些信号输出模式不能同时实现更快的信号输出、更准确和可靠的性能以及信号放大。核酶是一种具有高度结构和催化活性的 RNA 分子,能够特异性识别和切割特定的底物序列。在这里,我们采用核酶作为信号输出,开发了一种与核酶切割反应偶联的无细胞生物传感遗传电路,实现了对小分子的快速和灵敏检测。更重要的是,我们还成功构建了 3D 打印传感器阵列,从而实现了对抑制药物的高通量分析。此外,我们的方法将有助于扩展核酶在合成生物学领域的应用范围,并优化无细胞生物传感的信号输出系统,从而促进无细胞合成生物学在生物医学研究、临床诊断、环境监测和食品检测等领域的发展。