Liu Yaru, Li Yang, Gong Hao, Liu Yao, Wang Yijie, Ma Cuiping, Wei Yuxi, Shi Chao
Nucleic Acid Rapid Testing International Science and Technology Cooperation Base, College of Life Sciences, Qingdao University, 266071, Qingdao, People's Republic of China.
Sino-UAE International Cooperative Joint Laboratory of Pathogenic Microorganism Rapid Detection, Qingdao Nucleic Acid Rapid Detection Engineering Research Center, Qingdao Key Laboratory of Nucleic Acid Rapid Detection, College of Biological Engineering,, Qingdao University of Science and Technology, Qingdao, 266042, People's Republic of China.
Mikrochim Acta. 2025 Apr 22;192(5):315. doi: 10.1007/s00604-025-07143-8.
An ultra-fast, easy-to-use and non-amplification electrochemical detection platform was constructed for microRNA (miRNA) detection. A set of label-free hairpin probes and capture probes were introduced to form a ternary complex, which could enhance the selectivity and stability of miRNA detection due to the ability of reducing non-specific bind with non-target and enhancing accessibility of target to probes. Moreover, the capture probe immobilization and hybridization process were accelerated by the external electric field, shortening the detection time from 2 h to 5 min. The platform showed a detection limit of 1.28 fM under ideal experimental control conditions and had ability to identify 1- or 2-nucleotide (nt) difference. In addition, the designed sensor achieved the sensitive determination of miRNA-21 in serum samples. The excellent anti-interference capability of this detection method indicated its potential for clinical application. Its simplicity and high specificity made this method a promising tool for detecting different miRNA to assist the diagnosis of diverse cancers.
构建了一种用于微小RNA(miRNA)检测的超快速、易于使用且无需扩增的电化学检测平台。引入了一组无标记的发夹探针和捕获探针以形成三元复合物,由于其具有减少与非靶标的非特异性结合以及增强靶标与探针的可及性的能力,这可以提高miRNA检测的选择性和稳定性。此外,外部电场加速了捕获探针的固定和杂交过程,将检测时间从2小时缩短至5分钟。在理想的实验控制条件下,该平台的检测限为1.28 fM,并且能够识别1个或2个核苷酸(nt)的差异。此外,所设计的传感器实现了血清样本中miRNA-21的灵敏测定。这种检测方法出色的抗干扰能力表明了其临床应用潜力。其简单性和高特异性使该方法成为检测不同miRNA以辅助多种癌症诊断的有前景的工具。