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光笼扩增 FRET 纳米耀斑:时空可控的基于 mRNA 的纳米机器,用于活细胞中精确和灵敏的 microRNA 成像。

Photocaged amplified FRET nanoflares: spatiotemporal controllable of mRNA-powered nanomachines for precise and sensitive microRNA imaging in live cells.

机构信息

State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Key Laboratory for Bio-Nanotechnology and Molecular Engineering of Hunan Province, Hunan University, Changsha, P.R. China.

School of Chemistry and Chemical Engineering, Yangzhou University, Yangzhou, P.R. China.

出版信息

Nucleic Acids Res. 2022 Apr 22;50(7):e40. doi: 10.1093/nar/gkab1258.

Abstract

There is considerable interest in creating a precise and sensitive strategy for in situ visualizing and profiling intracellular miRNA. Present here is a novel photocaged amplified FRET nanoflare (PAFN), which spatiotemporal controls of mRNA-powered nanomachine for precise and sensitive miRNA imaging in live cells. The PAFN could be activated remotely by light, be triggered by specific low-abundance miRNA and fueled by high-abundance mRNA. It offers high spatiotemporal control over the initial activity of nanomachine at desirable time and site, and a 'one-to-more' ratiometric signal amplification model. The PAFN, an unprecedented design, is quiescent during the delivery process. However, upon reaching the interest tumor site, it can be selectively activated by light, and then be triggered by specific miRNA, avoiding undesirable early activation and reducing nonspecific signals, allowing precise and sensitive detection of specific miRNA in live cells. This strategy may open new avenues for creating spatiotemporally controllable and endogenous molecule-powered nanomachine, facilitating application at biological and medical imaging.

摘要

人们对于开发一种精确且灵敏的策略,用于在体内可视化和分析细胞内 miRNA 有着浓厚的兴趣。这里介绍了一种新型的光笼放大荧光共振能量转移纳米耀斑(PAFN),它是一种基于 mRNA 驱动的纳米机器,用于在活细胞中进行精确和灵敏的 miRNA 成像。PAFN 可以通过光远程激活,被特定低丰度 miRNA 触发,并由高丰度 mRNA 提供燃料。它提供了对纳米机器初始活性的高度时空控制,以及一种“一对一多”的比率信号放大模型。PAFN 是一种前所未有的设计,在递送过程中处于静止状态。然而,一旦到达感兴趣的肿瘤部位,它可以被光选择性地激活,然后被特定的 miRNA 触发,避免不必要的早期激活并减少非特异性信号,从而可以在活细胞中精确和灵敏地检测特定的 miRNA。该策略可能为创建时空可控和内源性分子驱动的纳米机器开辟新途径,有助于在生物和医学成像中的应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e97/9023253/482226684e11/gkab1258figgra1.jpg

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