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基于人工动态结构集合引导的通用RNA适配体传感标签的合理设计。

Artificial dynamic structure ensemble-guided rational design of a universal RNA aptamer-based sensing tag.

作者信息

Hou Jianing, Guo Pei, Wang Junyan, Han Da, Tan Weihong

机构信息

Institute of Molecular Medicine, Renji Hospital, School of Medicine Shanghai Jiao Tong University, Shanghai 200127, China.

Hangzhou Institute of Medicine, Chinese Academy of Sciences, Hangzhou, Zhejiang 310022, China.

出版信息

Proc Natl Acad Sci U S A. 2024 Dec 24;121(52):e2414793121. doi: 10.1073/pnas.2414793121. Epub 2024 Dec 20.

Abstract

Artificially functional RNAs, such as fluorogenic RNA aptamer (FRApt)-based biosensing tag, represent significant advancements in various biological applications but are limited by the lack of insight into dynamic structure ensembles and universal design concepts. Through the development of an artificial RNA structure ensemble, we rationally established an RNA reconstitution model, "SSPepper-Apt," to generate a universal fluorogenic RNA biosensing tag. By utilizing various target-recognizing RNA motifs, SSPepper-Apt enables the modular generation of sensing tags for low-background, highly selective imaging of metabolites, peptides, and proteins in living cells. Additionally, by employing single guide RNA (sgRNA) as the recognition RNA motif, SSPepper-Apt generates fluorescence in both CRISPR-mediated imaging and gene editing only when the Cas9-sgRNA complex is successfully assembled; therefore, it can be an effective sgRNA screening tool for gene editing. Our fluorogenic RNA-sensing tag provides a universal approach for constructing functional RNA systems, avoiding the laborious and time-consuming process of sequence combination, and expanding the application of synthetic biological tools.

摘要

人工合成的功能性RNA,如基于荧光RNA适体(FRApt)的生物传感标签,在各种生物学应用中取得了重大进展,但由于缺乏对动态结构集合和通用设计概念的深入了解而受到限制。通过开发一种人工RNA结构集合,我们合理地建立了一个RNA重组模型“SSPepper-Apt”,以生成通用的荧光RNA生物传感标签。通过利用各种靶标识别RNA基序,SSPepper-Apt能够模块化生成传感标签,用于对活细胞中的代谢物、肽和蛋白质进行低背景、高选择性成像。此外,通过使用单向导RNA(sgRNA)作为识别RNA基序,SSPepper-Apt仅在Cas9-sgRNA复合物成功组装时才会在CRISPR介导的成像和基因编辑中产生荧光;因此,它可以成为一种有效的基因编辑sgRNA筛选工具。我们的荧光RNA传感标签为构建功能性RNA系统提供了一种通用方法,避免了序列组合的繁琐和耗时过程,并扩展了合成生物学工具的应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61a6/11670126/ccf0ad466fa7/pnas.2414793121fig01.jpg

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