Key Laboratory of Luminescent and Real-Time Analytical Chemistry (Southwest University), Ministry of Education, School of Chemistry and Chemical Engineering, Southwest University, Chongqing 400715, PR China.
Key Laboratory of Luminescent and Real-Time Analytical Chemistry (Southwest University), Ministry of Education, School of Chemistry and Chemical Engineering, Southwest University, Chongqing 400715, PR China.
Biosens Bioelectron. 2018 Nov 15;119:170-175. doi: 10.1016/j.bios.2018.08.006. Epub 2018 Aug 8.
In this study, an electrochemical biosensor was proposed for microRNA-21 detection based on FeO/CeO @Au magnetite nanoparticles (FeO/CeO @Au MNPs) as nanocatalyst and catalytic hairpin assembly (CHA) for signal application. Firstly, target microRNA-21 hybridized with hairpin H to form H-T duplex stranded DNA (dsDNA), which could further open the hairpin H for the formation of H-H dsDNA. Simultaneously, the FeO/CeO @Au-S not only hybridized with single stranded fragment of H-H dsDNA with producing long dsDNA to absorb a large amount of electroactive substances of methylene blue (MB), but also acted as nanocatalyst to directly catalyze the reduction of MB for amplifying the electrochemical signal. Herein, compared with pure FeO nanoparticles, FeO/CeO @Au MNPs exhibited excellent catalytic performance since the cerium oxide (CeO) nanoparticles and Au nanoparticles can greatly improve the catalytic activity of FeO nanoparticles and effectively prevent the agglomeration of FeO nanoparticles. Owing to the signal amplification strategy, the proposed biosensor provided a wide linear range of 1 fM to 1 nM with a low detection limit of 0.33 fM (defined as S/N = 3) for microRNA-21 detection, and exhibited excellent specificity and sensitivity. This strategy provided a novel avenue for the detection of other biomarkers in electrochemical biosensors.
在这项研究中,基于 FeO/CeO@Au 磁性纳米粒子 (FeO/CeO@Au MNPs) 作为纳米催化剂和催化发夹组装 (CHA) 用于信号应用,提出了一种用于 microRNA-21 检测的电化学生物传感器。首先,靶 microRNA-21 与发夹 H 杂交形成 H-T 双链 DNA(dsDNA),其可进一步打开发夹 H 以形成 H-H dsDNA。同时,FeO/CeO@Au-S 不仅与 H-H dsDNA 的单链片段杂交,产生长 dsDNA 以吸收大量的电活性物质亚甲基蓝 (MB),而且还充当纳米催化剂,直接催化 MB 的还原以放大电化学信号。与纯 FeO 纳米粒子相比,FeO/CeO@Au MNPs 表现出优异的催化性能,因为氧化铈 (CeO) 纳米粒子和 Au 纳米粒子可以极大地提高 FeO 纳米粒子的催化活性,并有效防止 FeO 纳米粒子的聚集。由于信号放大策略,所提出的生物传感器在 microRNA-21 检测中提供了 1 fM 至 1 nM 的宽线性范围和 0.33 fM 的低检测限 (定义为 S/N=3),表现出优异的特异性和灵敏度。该策略为电化学生物传感器中其他生物标志物的检测提供了新途径。