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基于自供电和自反馈熵驱动的催化剂-DNA 酶电路的细胞内 miRNA 成像。

Intracellular miRNA Imaging Based on a Self-Powered and Self-Feedback Entropy-Driven Catalyst-DNAzyme Circuit.

机构信息

Fujian Key Laboratory of Functional Marine Sensing Materials, Center for Advanced Marine Materials and Smart Sensors, College of Materials and Chemical Engineering, Minjiang University, Fuzhou 350108, P. R. China.

College of Chemistry, Fuzhou University, Fuzhou 350116, P. R. China.

出版信息

ACS Appl Mater Interfaces. 2022 Sep 7;14(35):39866-39872. doi: 10.1021/acsami.2c11923. Epub 2022 Aug 26.

Abstract

DNAzyme-based signal amplification circuits promote the advances in low-abundant miRNA imaging in living cells. However, due to the insufficient cofactor in living cells and unsustainable target utilization, self-powered and self-feedback DNAzyme amplification circuits have rarely been achieved. Here, a MnO nanosheet-mediated self-powered and self-feedback entropy-driven catalyst (EDC)-DNAzyme nanoprobe (MnPFEDz) was demonstrated for sensitive imaging of intracellular microRNA (miRNA). In this strategy, MnPFEDz was formed by adsorbing EDC modules and substrate probes on MnO nanosheets. The MnO nanosheets acted not only as glutathione (GSH)-responsive nanocarriers for efficient delivery of DNA probes but also as a DNAzyme cofactor supplier to power the DNAzyme biocatalysis and promote signal transduction in a feedback way. When entering the cells, GSH could decompose MnO nanosheets to generate numerous Mn ion cofactors, leading to the release of DNA probes. Subsequently, the target miRNA initiated EDC cycles to generate amplified fluorescence signals and exposed the complete DNAzyme. Meanwhile, each of the exposed DNAzyme then cleaved the substrate probes with the help of Mn ion cofactors and released a new trigger analogue for the next round of EDC cycles, initiating additional fluorescence signals in a feedback way. As a multiple signal amplification strategy, the MnPFEDz nanoprobe facilitated the effective detection of intracellular molecules with enhanced sensitivity and provided a versatile strategy for the construction of self-powered and self-feedback DNA circuits in living cells.

摘要

基于 DNA 酶的信号扩增电路促进了低丰度 miRNA 在活细胞中成像的进展。然而,由于活细胞中辅助因子不足和目标利用不可持续,自供电和自反馈 DNA 酶扩增电路很少实现。在这里,展示了一种 MnO 纳米片介导的自供电和自反馈熵驱动催化剂 (EDC)-DNA 酶纳米探针 (MnPFEDz),用于灵敏地成像细胞内 microRNA (miRNA)。在该策略中,MnO 纳米片通过吸附 EDC 模块和底物探针形成 MnPFEDz。MnO 纳米片不仅作为谷胱甘肽 (GSH) 响应性纳米载体,用于高效递送 DNA 探针,还作为 DNA 酶辅助因子的供应源,以自供电的方式驱动 DNA 酶生物催化,并以反馈的方式促进信号转导。进入细胞后,GSH 可分解 MnO 纳米片生成大量 Mn 离子辅助因子,导致 DNA 探针释放。随后,目标 miRNA 启动 EDC 循环生成放大的荧光信号并暴露完整的 DNA 酶。同时,每个暴露的 DNA 酶在 Mn 离子辅助因子的帮助下切割底物探针,并释放新的触发类似物,用于下一轮 EDC 循环,以反馈的方式引发额外的荧光信号。作为一种多重信号扩增策略,MnPFEDz 纳米探针促进了细胞内分子的有效检测,具有增强的灵敏度,并为在活细胞中构建自供电和自反馈 DNA 电路提供了一种通用策略。

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