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在……中使用 toehold 传感器检测岛状 mRNA

Detection of Island mRNAs Using Toehold Sensors in .

作者信息

Heo Taeyang, Kang Hansol, Choi Seungdo, Kim Jongmin

机构信息

Department of Life Sciences, Pohang University of Science and Technology, Pohang 37673, Korea.

出版信息

Life (Basel). 2021 Nov 22;11(11):1280. doi: 10.3390/life11111280.

Abstract

Synthetic biologists have applied biomolecular engineering approaches toward the goal of novel biological devices and have shown progress in diverse areas of medicine and biotechnology. Especially promising is the application of synthetic biological devices towards a novel class of molecular diagnostics. As an example, a de-novo-designed riboregulator called toehold switch, with its programmability and compatibility with field-deployable devices showed promising in vitro applications for viral RNA detection such as Zika and Corona viruses. However, the in vivo application of high-performance RNA sensors remains challenging due to the secondary structure of long mRNA species. Here, we introduced 'Helper RNAs' that can enhance the functionality of toehold switch sensors by mitigating the effect of secondary structures around a target site. By employing the helper RNAs, previously reported mRNA sensor showed improved fold-changes in vivo. To further generalize the Helper RNA approaches, we employed automatic design pipeline for toehold sensors that target the essential genes within the island, an important target of biomedical research in connection with colorectal cancer. The toehold switch sensors showed fold-changes upon the expression of full-length mRNAs that apparently depended sensitively on the identity of the gene as well as the predicted local structure within the target region of the mRNA. Still, the helper RNAs could improve the performance of toehold switch sensors in many instances, with up to 10-fold improvement over no helper cases. These results suggest that the helper RNA approaches can further assist the design of functional RNA devices in vivo with the aid of the streamlined automatic design software developed here. Further, our solutions for screening and stabilizing single-stranded region of mRNA may find use in other in vivo mRNA-sensing applications such as cas13 crRNA design, transcriptome engineering, and trans-cleaving ribozymes.

摘要

合成生物学家已将生物分子工程方法应用于新型生物装置的研发,并在医学和生物技术的多个领域取得了进展。合成生物装置在新型分子诊断中的应用尤其具有前景。例如,一种名为“支点开关”的全新设计的核糖调节因子,因其可编程性以及与现场可部署设备的兼容性,在寨卡病毒和冠状病毒等病毒RNA检测的体外应用中显示出了潜力。然而,由于长mRNA物种的二级结构,高性能RNA传感器的体内应用仍然具有挑战性。在此,我们引入了“辅助RNA”,它可以通过减轻靶位点周围二级结构的影响来增强支点开关传感器的功能。通过使用辅助RNA,先前报道的mRNA传感器在体内显示出了更好的倍数变化。为了进一步推广辅助RNA方法,我们采用了针对岛内必需基因的支点传感器自动设计流程,该岛是与结直肠癌相关的生物医学研究的一个重要靶点。支点开关传感器在全长mRNA表达时显示出倍数变化,这显然敏感地依赖于基因的身份以及mRNA靶区域内预测的局部结构。尽管如此,辅助RNA在许多情况下仍可提高支点开关传感器的性能,比无辅助情况提高了多达10倍。这些结果表明,辅助RNA方法可以借助此处开发的简化自动设计软件,进一步协助体内功能性RNA装置的设计。此外,我们用于筛选和稳定mRNA单链区域的解决方案可能会用于其他体内mRNA传感应用,如cas13 crRNA设计、转录组工程和反式切割核酶。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5307/8625898/9f7acdf2a896/life-11-01280-g001.jpg

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