School of Chemistry, Guangzhou Key Laboratory of Analytical Chemistry for Biomedicine, South China Normal University, Guangzhou, 510006, People's Republic of China.
School of Environmental and Chemical Engineering, Key Laboratory of Jiangxi Province for Persistent Pollutants Control and Resources Recycle, Nanchang Hangkong University, Nanchang, 330063, People's Republic of China.
Mikrochim Acta. 2023 Mar 23;190(4):149. doi: 10.1007/s00604-023-05720-3.
An electrochemical strategy based on bimetallic nanozyme in collaboration with toehold-mediated DNA replacement effect is proposed for the sensitive determination of miRNA-21. The AuPt nanoparticles (AuPt NPs) are prepared as a catalytic beacon; it shows favorable peroxidase properties with a Michaelis contant (K) of 0.072 mM for HO, which is capable of catalyzing HO to induce an intense redox reaction, and causing a measurable electrochemical signal. To further enhance the strength of the signal response, a novel toehold-mediated DNA replacement strategy is employed. DNA strands with specific sequences are modified on electrodes and AuPt NPs, respectively. In the presence of miRNA-21, a cyclic substitution effect is subsequently activated via a specific toehold sequence and leads to a large accumulation of AuPt NPs on the electrodes. Subsequently, a strong signal depending on the amount of miRNA-21 is obtained after adding a small amount of HO. The analytical range of this determination method is from 0.1 pM to 1.0 nM, and the LOD is 84.1 fM. The spike recoveries for serum samples are 95.0 to 102.4% and the RSD values are 3.7 to 5.8%. The results suggests a promising application of the established method in clinical testing and disease diagnosis.
基于双金属纳米酶与引发链置换效应协同作用的电化学生物传感器用于 miRNA-21 的灵敏检测。制备了金铂纳米颗粒(AuPt NPs)作为催化信标;它表现出良好的过氧化物酶性质,HO 的米氏常数(K)为 0.072 mM,能够催化 HO 诱导强烈的氧化还原反应,并产生可测量的电化学信号。为了进一步增强信号响应强度,采用了一种新颖的引发链置换策略。具有特定序列的 DNA 链分别修饰在电极和 AuPt NPs 上。在存在 miRNA-21 的情况下,通过特定的引发序列激活循环取代效应,导致大量 AuPt NPs 聚集在电极上。随后,加入少量 HO 后,会得到一个依赖于 miRNA-21 量的强信号。该测定方法的分析范围为 0.1 pM 至 1.0 nM,LOD 为 84.1 fM。血清样品的加标回收率为 95.0%至 102.4%,RSD 值为 3.7%至 5.8%。结果表明,所建立的方法在临床检测和疾病诊断中具有广阔的应用前景。