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基于超支化杂交链式反应驱动的空间局域化 DNA 纳米机器对环境铅离子的无标记和超高灵敏检测。

Label-free and ultrasensitive detection of environmental lead ions based on spatially localized DNA nanomachines driven by hyperbranched hybridization chain reaction.

机构信息

State Key Laboratory of Food Nutrition and Safety, Key Laboratory of Food Nutrition and Safety (Ministry of Education), College of Food Engineering and Biotechnology, Tianjin University of Science & Technology, Tianjin 300457, PR China.

Life and Health Research Institute School of Chemistry and Chemical Engineering, Tianjin University of Technology, Tianjin 300384, PR China.

出版信息

J Hazard Mater. 2024 Sep 5;476:135115. doi: 10.1016/j.jhazmat.2024.135115. Epub 2024 Jul 5.

DOI:10.1016/j.jhazmat.2024.135115
PMID:38976962
Abstract

A label-free fluorescent sensing strategy for the rapid and highly sensitive detection of Pb was developed by integrating Pb DNAzyme-specific cleavage activity and a tetrahedral DNA nanostructure (TDN)-enhanced hyperbranched hybridization chain reaction (hHCR). This strategy provides accelerated reaction rates because of the highly effective collision probability and enriched local concentrations from the spatial confinement of the TDN, thus showing a higher detection sensitivity and a more rapid detection process. Moreover, a hairpin probe based on a G-triplex instead of a G-quadruplex or chemical modification makes hybridization chain reaction more controlled and flexible, greatly improving signal amplification capacities and eliminating labeled DNA probes. The enhanced reaction rates and improved signal amplification efficiency endowed the biosensors with high sensitivity and a rapid response. The label-free detection of Pb based on G-triplex combined with thioflavin T can be achieved with a detection limit as low as 1.8 pM in 25 min. The proposed Pb-sensing platform was also demonstrated to be applicable for Pb detection in tap water, river water, shrimp, rice, and soil samples, thus showing great potential for food safety and environmental monitoring.

摘要

一种无标记荧光传感策略通过整合 Pb DNA 酶特异性切割活性和四面体 DNA 纳米结构(TDN)增强的超支化杂交链式反应(hHCR),用于快速、高灵敏地检测 Pb。由于 TDN 的空间限制,该策略提供了更快的反应速率,具有更高的检测灵敏度和更快的检测过程,因为其具有极高的有效碰撞概率和丰富的局部浓度。此外,基于 G-三链体而不是 G-四链体或化学修饰的发夹探针使杂交链式反应更具可控性和灵活性,大大提高了信号放大能力并消除了标记的 DNA 探针。更快的反应速率和改进的信号放大效率使生物传感器具有高灵敏度和快速响应。基于 G-三链体与硫堇 T 的无标记 Pb 检测可在 25 分钟内实现低至 1.8 pM 的检测限。所提出的基于 Pb 感应的平台还可用于检测自来水中、河水、虾、大米和土壤样本中的 Pb,因此在食品安全和环境监测方面具有很大的应用潜力。

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