Department of Clinical Laboratory, Nanjing Gaochun People's Hospital, Nanjing, 211300, PR China.
Women's Hospital of Nanjing Medical University, Nanjing Maternity and Child Health Care Hospital, Nanjing, 210004, PR China.
Talanta. 2020 Nov 1;219:121242. doi: 10.1016/j.talanta.2020.121242. Epub 2020 Jun 13.
Growing evidence suggests that exosomes-encapsulated miRNAs detection is of paramount significance in early diagnostics of cancer due to protection from degradation by ribonuclease. However, exosomal microRNAs with low abundance and subtle variation have restricted their clinical application. Herein, an electrochemical biosensor for highly sensitive detection of exosomal microRNAs has been fabricated based on the double signal amplification strategy. Our proposed amplifier consists of two steps: target miRNA cyclic signal amplification induced by strand displacement reaction (SDR) and subsequent deposition of silver nanoparticles induced by streptavidin-biotin interaction. Consequently, this method shows ultrahigh sensitivity to detect miRNA. Taking miRNA-21 in exosomes as a model analyte, a detection limit of 0.4 fM (S/N = 3) can be obtained. Meanwhile, the method is relatively simple and low-cost without the requirement of enzyme, which has been applied in biological samples successfully. Therefore, our miRNA assay method has shown great promise as molecular tool in the detection of exosomal miRNA and could be widely used in clinic in the future.
越来越多的证据表明,由于 exosomes 包裹的 miRNAs 受到核糖核酸酶的保护,不易降解,因此其检测在癌症的早期诊断中具有至关重要的意义。然而,由于 exosomal microRNAs 丰度低且变化细微,其临床应用受到限制。本文基于双信号放大策略,构建了一种用于高灵敏度检测 exosomal microRNAs 的电化学生物传感器。我们提出的放大器由两个步骤组成:链置换反应(SDR)诱导的靶 miRNA 循环信号放大和随后的链霉亲和素-生物素相互作用诱导的银纳米粒子沉积。因此,该方法对 miRNA 的检测具有超高灵敏度。以 exosomes 中的 miRNA-21 为模型分析物,可得到 0.4 fM 的检测限(S/N = 3)。同时,该方法相对简单且成本低,无需酶,已成功应用于生物样品。因此,我们的 miRNA 检测方法作为检测 exosomal miRNA 的分子工具具有很大的应用前景,有望在未来得到广泛应用。