Target-promoted autocatalytic hairpin assembly of bivalent DNAzymes for sensitive and label-free electrochemical metallothionein assay

被引:1
|
作者
Yao, Jianglong [1 ]
Liu, Yujie [1 ]
Li, Daxiu [2 ]
Jiang, Bingying [1 ]
Xiang, Yun [3 ]
Yuan, Ruo [3 ]
机构
[1] Chongqing Univ Technol, Sch Chem & Chem Engn, Chongqing 400054, Peoples R China
[2] Chongqing Univ Technol, Coll Pharm & Biol Engn, Chongqing 400054, Peoples R China
[3] Southwest Univ, Sch Chem & Chem Engn, Key Lab Luminescence Anal & Mol Sensing, Minist Educ, Chongqing 400715, Peoples R China
基金
中国国家自然科学基金;
关键词
Metallothionein; Autocatalytic hairpin assembly; DNAzyme; Label; -free; Electrochemical biosensor; PERFORMANCE LIQUID-CHROMATOGRAPHY; FLIGHT MASS-SPECTROMETRY; DUAL-CHANNEL DETECTION; SPECIATION ANALYSIS; FLUORESCENCE; AMPLIFICATION; BIOSENSOR;
D O I
10.1016/j.talanta.2024.126398
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Metallothionein (MT) has shown to be an important biomarker for environmental monitoring and various diseases, due to its significant binding ability to heavy metal ions. On the basis of such a characteristic and the Hg2+stabilized DNA duplex (Hg2+-dsDNA) probe, as well as a new autocatalytic hairpin assembly (aCHA)/DNAzyme cascaded signal enhancement strategy, the construction of a highly sensitive and label-free electrochemical MT biosensor is described. Target MT molecules bind Hg2+ in Hg2+-dsDNA to disrupt the duplex structure and to release ssDNA sequences, which trigger subsequent aCHA for efficient production of mimic aCHA triggering strands and many bivalent DNAzymes. The signal hairpins on the electrode are then cyclically cleaved by DNAzyme amplification cascade to liberate plenty G-quadruplex sequences, which bind hemin and yield largely enhanced currents for sensitive assay of MT with a detection limit of 0.217 nM in a label-free approach. Such sensor also shows selective discrimination capability to MT against other interfering proteins and assay of MT in normal serums with dilution has also been verified, indicating its potential for highly sensitive detection of different heavy metal ion binding molecules for various application scenarios.
引用
收藏
页数:6
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