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六分支 DNA 纳米轮诱导核酸限域效应的近红外光控荧光纳米传感器用于高性能生物成像。

NIR Photocontrolled Fluorescent Nanosensor under a Six-Branched DNA Nanowheel-Induced Nucleic Acid Confinement Effect for High-Performance Bioimaging.

机构信息

School of Public Health, Wuhan University of Science and Technology, Wuhan 430065, P. R. China.

School of Basic Medical Sciences, Biomedical Research Institute, Hubei University of Medicine, Shiyan 442000, P. R. China.

出版信息

ACS Appl Mater Interfaces. 2023 Mar 1;15(8):10529-10540. doi: 10.1021/acsami.2c23165. Epub 2023 Feb 20.

DOI:10.1021/acsami.2c23165
PMID:36802484
Abstract

Although DNA nanotechnology is a promising option for fluorescent biosensors to perform bioimaging, the uncontrollable target identification during biological delivery and the spatially free molecular collision of nucleic acids may cause unsatisfactory imaging precision and sensitivity, respectively. Aiming at solving these challenges, we herein integrate some productive notions. On the one hand, the target recognition component is inserted with a photocleavage bond and a core-shell structured upconversion nanoparticle with a low thermal effect is further employed to act as the ultraviolet light generation source, under which a precise near-infrared photocontrolled sensing is achieved through a simple external 808 nm light irradiation. On the other hand, the collision of all of the hairpin nucleic acid reactants is confined by a DNA linker to form a six-branched DNA nanowheel, after which their local reaction concentrations are vastly enhanced (∼27.48 times) to induce a special nucleic acid confinement effect to guarantee highly sensitive detection. By selecting a lung cancer-associated short noncoding microRNA sequence (miRNA-155) as a model low-abundance analyte, it is demonstrated that the newly established fluorescent nanosensor not only presents good assay performance but also exhibits a high-performance bioimaging competence in live biosystems including cells and mouse body, propelling the progress of DNA nanotechnology in the biosensing field.

摘要

尽管 DNA 纳米技术是荧光生物传感器进行生物成像的一种很有前途的选择,但在生物传递过程中目标识别不可控,以及核酸的空间自由分子碰撞,可能分别导致成像精度和灵敏度不理想。针对这些挑战,我们整合了一些有成效的概念。一方面,将目标识别组件插入光裂解键,并进一步采用具有低热效应的核壳结构上转换纳米粒子作为紫外光发生源,在这种情况下,通过简单的外部 808nm 光照射,可以实现精确的近红外光控感应。另一方面,通过 DNA 接头将所有发夹核酸反应物的碰撞限制在一个六分支 DNA 纳米轮内,从而大大提高了它们的局部反应浓度(约 27.48 倍),以诱导特殊的核酸限制效应,保证高灵敏度检测。通过选择一个与肺癌相关的短非编码 microRNA 序列(miRNA-155)作为模型低丰度分析物,证明了新建立的荧光纳米传感器不仅具有良好的分析性能,而且在包括细胞和小鼠体在内的活体生物系统中表现出高性能的生物成像能力,推动了 DNA 纳米技术在生物传感领域的发展。

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