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一种用于精确灵敏的微小RNA成像的近红外响应光笼放大DNA纳米器件。

A near-infrared responsive photocaged amplified DNA nanodevice for precise and sensitive microRNA imaging.

作者信息

Zhong Yan, Li Zheng, Li Bo, Xu Chang, Bai Tuya, Qian Hang, Wang Chunyan

机构信息

Department of Chemistry and Chemical Engineering, Inner Mongolia University, Hohhot, 010020, China.

Department of Respiratory and Critical Care Medicine, Second Affiliated Hospital of Third Military Medical University (Army Medical University), Chongqing, 400037, China.

出版信息

Mater Today Bio. 2025 Aug 16;34:102208. doi: 10.1016/j.mtbio.2025.102208. eCollection 2025 Oct.

Abstract

MicroRNAs (miRNAs) play a critical role in early cancer detection, but traditional DNA probes are limited by the low abundance of miRNAs and their "always effective" property. Herein, we construct a photocaged amplified DNA nanodevice (PAD) by attaching DNA probes to upconversion nanoparticles (UCs). Upon remote near-infrared (NIR) light stimulation, the photocleavable DNA probes are activated by emitted UV light, and subsequently triggered by target miRNA. This process is further propelled by mRNA and DNA hairpin to achieve "one to many" signal amplification, enabling precise and sensitive spatiotemporal resolved imaging of miRNA. results demonstrate that the proposed dual-cycle amplification strategy effectively prevents undesired activation and minimizes non-specific signals, achieving a remarkable 20-fold improvement in miRNA detection limit compared to the one-cycle amplification strategy. Additionally, PAD enables spatiotemporally controlled miRNA imaging in tumor-bearing mouse models through NIR light-regulated activation. The proposed approach extends the application of light-gated spatiotemporal controllable DNA nanodevice in nucleic acid imaging, thereby advancing its application in biological and medical imaging.

摘要

微小RNA(miRNA)在癌症早期检测中起着关键作用,但传统的DNA探针受到miRNA丰度低及其“始终有效”特性的限制。在此,我们通过将DNA探针连接到上转换纳米颗粒(UCs)上构建了一种光笼式扩增DNA纳米器件(PAD)。在远程近红外(NIR)光刺激下,可光裂解的DNA探针被发射的紫外光激活,随后被靶miRNA触发。这一过程通过mRNA和DNA发夹进一步推进,以实现“一对多”信号放大,从而实现对miRNA的精确和灵敏的时空分辨成像。结果表明,所提出的双循环扩增策略有效地防止了不必要的激活,并将非特异性信号降至最低,与单循环扩增策略相比,miRNA检测限显著提高了20倍。此外,PAD通过近红外光调节的激活,在荷瘤小鼠模型中实现了时空可控的miRNA成像。所提出的方法扩展了光门控时空可控DNA纳米器件在核酸成像中的应用,从而推动了其在生物和医学成像中的应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/641b/12396463/e31e66b644e6/ga1.jpg

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