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茶碱敏感型锤头状核酸适体的细胞内筛选

Intracellular Selection of Theophylline-Sensitive Hammerhead Aptazyme.

作者信息

Pu Qinlin, Zhou Shan, Huang Xin, Yuan Yi, Du Feng, Dong Juan, Chen Gangyi, Cui Xin, Tang Zhuo

机构信息

Natural Products Research Center, Chengdu Institution of Biology, Chinese Academy of Science, Chengdu 610041, P.R. China; University of Chinese Academy of Sciences, Beijing 10049, P.R. China.

Natural Products Research Center, Chengdu Institution of Biology, Chinese Academy of Science, Chengdu 610041, P.R. China.

出版信息

Mol Ther Nucleic Acids. 2020 Jun 5;20:400-408. doi: 10.1016/j.omtn.2020.03.001. Epub 2020 Mar 13.

Abstract

Hammerhead ribozyme-based aptazyme (HHAz), inheriting the advantages of small size and high efficiency from the RNA-cleaving ribozyme and the specific recognition ability of aptamers to specific targets, exhibits the huge potential to be a transgene expression regulator. Herein, we report a selection strategy for HHAz by using a toxin protein IbsC as the reporter to offer a positive phenotype, thus realizing an easy-operating, time- and labor-saving selection of HHAz variants with desired properties. Based on this strategy, we obtained a new HHAz (TAP-1), which could react sensitively toward the extracellular regulatory molecule, theophylline, both in prokaryotic and eukaryotic systems. With fluorescent protein reporter, the intracellular switching efficiencies of TAP-1 and other reported theophylline-dependent HHAzs has been quantitatively evaluated, showing that TAP-1 not only exhibits the best downregulating ability at high concentration of theophylline but also maintains high activity with 0.1 mM theophylline, which is a safe concentration in the human body.

摘要

基于锤头状核酶的适体酶(HHAz)继承了RNA切割核酶体积小、效率高的优点以及适体对特定靶标的特异性识别能力,展现出作为转基因表达调节剂的巨大潜力。在此,我们报道了一种以毒素蛋白IbsC作为报告基因以提供阳性表型来筛选HHAz的策略,从而实现对具有所需特性的HHAz变体进行简便、省时省力的筛选。基于此策略,我们获得了一种新的HHAz(TAP-1),它在原核和真核系统中都能对细胞外调节分子茶碱做出灵敏反应。通过荧光蛋白报告基因,对TAP-1和其他已报道的茶碱依赖性HHAz的细胞内开关效率进行了定量评估,结果表明TAP-1不仅在高浓度茶碱下表现出最佳的下调能力,而且在0.1 mM茶碱(人体中的安全浓度)下也保持高活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c40/7118274/548ef39559fd/fx1.jpg

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