脱氧核酶
化学
细胞内
分析物
小RNA
基质(水族馆)
生物物理学
纳米技术
组合化学
DNA
材料科学
生物化学
生物
基因
生态学
物理化学
作者
Lei Yang,Qiong Wu,Yuqi Chen,Xiaoqing Liu,Fuan Wang,Xiang Zhou
出处
期刊:ACS Sensors
[American Chemical Society]
日期:2018-12-18
卷期号:4 (1): 110-117
被引量:97
标识
DOI:10.1021/acssensors.8b01000
摘要
Abnormal microRNAs (miRNAs) expression is demonstrated to associate with various important biological processes, including tumorigenesis, metastasis, and progression. Given the low miRNA expression at the earlier stage of diseases, its amplified detection still requires more efforts. Inspired by the two-stage arithmetic amplifier of electric devices, we reported an autonomous and catalytic assembly of DNAzyme strategy by integrating a DNAzyme biocatalyst and catalytic hairpin assembly (CHA) circuit. Here the catalytically inactive DNAzyme subunits were respectively grafted into these metastable CHA hairpin reactants that were kinetically impeded without false cross-hybridizations. The target catalyzed the nonenzymatic CHA-mediated successive assembly of dumbbell-like bis-DNAzyme nanostructures, leading to the efficient DNAzyme-mediated cleavage of fluorophore/quencher-modified substrate and to the generation of an amplified fluorescence signal. The present CHA-DNAzyme amplifier can be employed as a versatile and general sensing platform for analyzing other analytes (e.g., miRNA) by introducing a sensing module into the present system. Moreover, the homogeneous CHA-DNAzyme method could realize the sensitive intracellular miRNA imaging in living cells, which is attributed to the inherently synergistic amplification property between DNAzyme and CHA reactions. Given the attractive analytical features of the autonomous CHA-DNAzyme system, the present strategy shows great promise for analyzing additional different analytes in clinical research fields.
科研通智能强力驱动
Strongly Powered by AbleSci AI