Jiang Hong, Liu Xiao, Zhao Dong, Jia Yu-Kang, Wang Ya-Qin, Li Wei, Liu Zhao-Peng, Wang Ji-Dong
State Key Laboratory of Metastable Materials Science and Technology, Nano-Biotechnology Key Lab of Hebei Province, College of Environmental and Chemical Engineering, Yanshan University, Qinhuangdao 066004, China.
Anal Chem. 2024 Dec 31;96(52):20656-20664. doi: 10.1021/acs.analchem.4c05482. Epub 2024 Dec 19.
Microelectrode- and nanoelectrode-based electrochemistry has become a powerful tool for the in situ monitoring of various biomolecules in vivo. However, two challenges limit the application of micro- and nanoelectrodes: the difficulty of highly sensitive detection of nonelectroactive molecules and the specific detection of target molecules in complex biological environments. Herein, we propose an electrochemical microsensor based on an entropy-driven multipedal DNA walker for the highly sensitive and selective detection of ATP. An ATP aptamer was immobilized on the microelectrode surface to form the DNA walker track for selective ATP recognition. Multiple walking "legs" were attached to quantum dots to create the multipedal DNA walker. ATP was selectively captured by the ATP aptamer, triggering the autonomous movement of the multipedal DNA walker on the microelectrode interface, which brought methylene blue (MB) closer to the microelectrode interface, realizing a cascade signal amplification. Additionally, ATP release induced by hypotonic conditions in BV2 cells was successfully monitored, indicating that increased cell volume enhances ATP release. This multipedal DNA walker microsensor offers a novel strategy for in situ, highly sensitive, and selective monitoring of nonelectroactive biomolecules in vivo, which is crucial for investigating the neurochemical processes involved in neurological diseases.
基于微电极和纳米电极的电化学已成为体内各种生物分子原位监测的有力工具。然而,两个挑战限制了微电极和纳米电极的应用:非电活性分子高灵敏度检测的困难以及复杂生物环境中目标分子的特异性检测。在此,我们提出一种基于熵驱动多足DNA步行器的电化学微传感器,用于高灵敏度和选择性地检测ATP。将ATP适配体固定在微电极表面,形成用于选择性识别ATP的DNA步行器轨道。多个行走“腿 ”连接到量子点上,构建多足DNA步行器。ATP被ATP适配体选择性捕获,触发多足DNA步行器在微电极界面上的自主移动,使亚甲基蓝(MB)更靠近微电极界面,实现级联信号放大。此外,成功监测了低渗条件下BV2细胞诱导的ATP释放,表明细胞体积增加会增强ATP释放。这种多足DNA步行器微传感器为体内非电活性生物分子的原位、高灵敏度和选择性监测提供了一种新策略,这对于研究神经疾病中涉及的神经化学过程至关重要。