Zhan Jiajun, Wang Futing, Li Yujin, Li Jingxian, Hong Chengyi, Yang Hongfen, Yang Dan, Cai Ren
Molecular Science and Biomedicine Laboratory, State Key Laboratory for Chemo/Bio-Sensing and Chemometrics, College of Material Science and Engineering, Hunan University, Changsha, 410082, China.
College of Ocean Food and Biological Engineering, Fujian Provincial Key Laboratory of Food Microbiology and Enzyme Engineering, Jimei University, Xiamen, 361021, China.
Anal Chim Acta. 2025 Oct 1;1369:344346. doi: 10.1016/j.aca.2025.344346. Epub 2025 Jun 19.
MicroRNAs (miRNAs), a type of small non-coding RNA sequences, are very important biomarkers and are involved in various physiological processes, such as cell proliferation, growth, differentiation, and apoptosis. Many reports have shown that miRNAs are closely associated with a variety of diseases, including neurodegenerative diseases and cancer. Currently, researchers have developed various methods for miRNAs detection, such as fluorescence, surface-enhanced Raman scattering, electrochemiluminescence, and electrochemical sensing. The detection of multiple miRNAs is significant for the diagnosis of diseases. However, it is rare for a single biosensing system to ultra-sensitively detect multiple miRNAs.
Based on enzyme biofuel cells (EBFCs) and catalytic hairpin assembly (CHA), a novel self-powered biosensor is designed for the sequential ultra-sensitive detection of miRNA-21, miRNA-146a, miRNA-155. First, miRNA-21 initiates CHA, and hairpin-tetrahedral DNA nanostructure (H-TDN) is captured on the biocathode. As a result, the open-circuit voltage 1 (E) increases, i.e., a signal "on" state. Next, in the presence of miRNA-146a, another CHA process is activated, and DNA1-glucose oxidase (DNA1-GOD) is replaced by hairpin 2 (H2) on the bioanode. This causes the open-circuit voltage (E) to decrease, i.e., a signal "off" state. Finally, when miRNA-155 is present, DNA2-GOD is captured by miRNA-155. And E increases, i.e., a signal "on" state. Moreover, the self-powered biosensor possesses good selectivity, high reproducibility, and excellent stability for miRNAs assay.
Based on the variation of the open-circuit voltage, this novel self-powered biosensor exhibits ultra-highly sensitive detection for miRNA-21 with the limit of detection (LOD) of 0.36 fM, miRNA-146a with the LOD of 0.16 fM, and miRNA-155 with the LOD of 0.23 fM. This novel self-powered biosensor provides a feasible solution to explore ultra-sensitive sequential biosensors with multi-target detection.
微小RNA(miRNA)是一类小的非编码RNA序列,是非常重要的生物标志物,参与细胞增殖、生长、分化和凋亡等多种生理过程。许多报道表明,miRNA与包括神经退行性疾病和癌症在内的多种疾病密切相关。目前,研究人员已经开发出多种miRNA检测方法,如荧光、表面增强拉曼散射、电化学发光和电化学传感。多种miRNA的检测对疾病诊断具有重要意义。然而,单个生物传感系统超灵敏检测多种miRNA的情况很少见。
基于酶生物燃料电池(EBFC)和催化发夹组装(CHA),设计了一种新型自供电生物传感器,用于对miRNA-21、miRNA-146a、miRNA-155进行顺序超灵敏检测。首先,miRNA-21启动CHA,生物阴极捕获发夹-四面体DNA纳米结构(H-TDN)。结果,开路电压1(E)增加,即信号“开启”状态。接下来,在miRNA-146a存在的情况下,另一个CHA过程被激活,生物阳极上的DNA1-葡萄糖氧化酶(DNA1-GOD)被发夹2(H2)取代。这导致开路电压(E)降低,即信号“关闭”状态。最后,当存在miRNA-155时,DNA2-GOD被miRNA-155捕获。E增加,即信号“开启”状态。此外,该自供电生物传感器对miRNA检测具有良好的选择性、高重现性和出色的稳定性。
基于开路电压的变化,这种新型自供电生物传感器对miRNA-21表现出超高灵敏度检测,检测限(LOD)为0.36 fM,对miRNA-146a的LOD为0.16 fM,对miRNA-155的LOD为0.23 fM。这种新型自供电生物传感器为探索具有多靶点检测功能的超灵敏顺序生物传感器提供了一种可行的解决方案。