适体
检出限
荧光
化学
信号(编程语言)
小分子
生物物理学
纳米技术
组合化学
计算生物学
材料科学
生物
分子生物学
计算机科学
生物化学
物理
量子力学
色谱法
程序设计语言
作者
Sujing Wang,Xia Li,Bingying Jiang,Ruo Yuan,Yun Xiang
标识
DOI:10.1016/j.snb.2019.126929
摘要
Sensitive detection and quantification of cytokines can play important roles in immunology research and diseases diagnosis. In this regard, by using a new target-triggered programming of cascaded catalytic hairpin assembly (CHA) signal enhancement strategy, we have developed an enzyme-free approach for the highly sensitive detection of cytokines, where interferon-γ (IFN-γ) is selected as the target model molecule. IFN-γ associates with a hairpin aptamer probe and triggers a conformation change of the aptamer to expose an initiation sequence for the formation of three independent and cascaded CHA of four hairpins into dsDNAs, which results in drastically enhanced fluorescence recovery from the fluorescently quenched hairpin signal probes for detecting IFN-γ in a dynamic range between 0.001 and 50 nM with detection limit down to 0.6 pM. Furthermore, this elaborately designed signal amplified approach displays efficient selectivity for the target molecules and can realize the detection of IFN-γ in diluted human serums, demonstrating its potential for monitoring a variety of biomarkers with high sensitivity by using appropriate hairpin aptamer/target molecule pairs.
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