Institute of Biomedical Engineering, National Taiwan University, Taipei 106, Taiwan, ROC.
Department of Obstetrics and Gynecology, Mackay Memorial Hospital, Taipei 104, Taiwan, ROC; Department of Medicine, Mackay Medical College, Taipei 252, Taiwan, ROC; Mackay Junior College of Medicine, Nursing, and Management, Taipei 112, Taiwan, ROC.
Biosens Bioelectron. 2016 Apr 15;78:200-205. doi: 10.1016/j.bios.2015.11.051. Epub 2015 Nov 18.
A branched DNA amplification strategy was employed to design a colorimetric aptameric biosensor using unmodified gold nanoparticles (AuNPs). First, a programmed DNA dendritic nanostructure was formed using two double-stranded substrate DNAs and two single-stranded auxiliary DNAs as assembly components via a target-assisted cascade amplification reaction, and it was then captured by DNA sensing probe-stabilized AuNPs. The release of sensing probes from AuNPs led to the formation of unstable AuNPs, promoting salt-induced aggregation. By integrating the signal amplification capacity of the branched DNA cascade reaction and unmodified AuNPs as a sensing indicator, this amplified colorimetric sensing strategy allows protein detection with high sensitivity (at the femtomole level) and selectivity. The limit of detection of this approach for VEGF was lower than those of other aptamer-based detection methods. Moreover, this assay provides modification-free and enzyme-free protein detection without sophisticated instrumentation and might be generally applicable to the detection of other protein targets in the future.
采用分支 DNA 扩增策略,利用未经修饰的金纳米粒子(AuNPs)设计了比色适体生物传感器。首先,通过目标辅助级联扩增反应,使用两条双链底物 DNA 和两条单链辅助 DNA 作为组装组件形成程序化 DNA 树枝状纳米结构,然后通过 DNA 感应探针稳定的 AuNPs 捕获。从 AuNPs 上释放出感应探针会导致不稳定的 AuNPs 的形成,从而促进盐诱导的聚集。通过整合分支 DNA 级联反应的信号放大能力和未修饰的 AuNPs 作为传感指示剂,这种放大比色传感策略可以实现高灵敏度(飞摩尔水平)和选择性的蛋白质检测。该方法检测 VEGF 的检测限低于其他基于适体的检测方法。此外,该方法提供了无需修饰和酶的蛋白质检测,无需复杂的仪器,并且将来可能普遍适用于其他蛋白质靶标的检测。