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高保真成像细胞内 microRNA 的生物正交纳米探针。

High-fidelity imaging of intracellular microRNA a bioorthogonal nanoprobe.

机构信息

Center of Smart Laboratory and Molecular Medicine, School of Medicine, Chongqing University, Chongqing, 400044, P.R. China.

Key Laboratory for Biorheological Science and Technology of Ministry of Education, College of Bioengineering, Chongqing University, Chongqing, 400044, P.R. China.

出版信息

Analyst. 2023 Apr 11;148(8):1682-1693. doi: 10.1039/d3an00088e.

Abstract

The spatiotemporal visualization of intracellular microRNA (miRNA) plays a critical role in the diagnosis and treatment of malignant disease. Although DNAzyme-based biosensing has been regarded as the most promising candidate, inefficient analytical resolution is frequently encountered. Here, we propose a bioorthogonal approach toward high-fidelity imaging of intracellular miRNA by designing a multifunctional nanoprobe that integrates MnO nanosheet-mediated intracellular delivery and activation by a fat mass and obesity-associated protein (FTO)-switched positive feedback. MnO nanosheets facilitate nanoprobe delivery and intracellular DNAzyme cofactors are released upon glutathione-triggered reduction. Meanwhile, an m6A-caged DNAzyme probe could be bioorthogonally activated by intracellular FTO to eliminate potential off-target activation. Therefore, the activated DNAzyme probe and substrate probe could recognize miRNA to perform cascade signal amplification in the initiation of the release of Mn from MnO nanosheets. This strategy realized high-fidelity imaging of intracellular aberrant miRNA within tumor cells with a satisfactory detection limit of 9.7 pM, paving the way to facilitate clinical tumor diagnosis and prognosis monitoring.

摘要

细胞内 microRNA(miRNA)的时空可视化在恶性疾病的诊断和治疗中起着关键作用。尽管基于 DNAzyme 的生物传感已被认为是最有前途的候选方法,但经常遇到分析分辨率不高的问题。在这里,我们提出了一种生物正交方法,通过设计一种多功能纳米探针来实现细胞内 miRNA 的高保真成像,该探针集成了 MnO 纳米片介导的细胞内递药和由肥胖相关蛋白(FTO)开关的正反馈激活。MnO 纳米片有助于纳米探针的递药,并且谷胱甘肽触发还原后会释放细胞内 DNAzyme 辅因子。同时,m6A 封闭的 DNAzyme 探针可以被细胞内的 FTO 生物正交激活,以消除潜在的非靶标激活。因此,激活的 DNAzyme 探针和底物探针可以识别 miRNA,从而在 MnO 纳米片释放 Mn 的起始阶段进行级联信号放大。该策略实现了肿瘤细胞内异常 miRNA 的高保真成像,检测限低至 9.7 pM,为促进临床肿瘤诊断和预后监测铺平了道路。

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