Chronoamperometric interrogation of an electrochemical aptamer-based sensor with tetrahedral DNA nanostructure pendulums for continuous biomarker measurements

被引:1
|
作者
Wang, Yizhou [1 ]
Duan, Haowei [1 ,3 ]
Yalikun, Yaxiaer [2 ]
Cheng, Shaokoon [1 ]
Li, Ming [1 ,3 ]
机构
[1] Macquarie Univ, Sch Engn, Fac Sci & Engn, Sydney, NSW 2109, Australia
[2] Nara Inst Sci & Technol, Grad Sch Sci & Technol, Div Mat Sci, Ikoma 6300192, Japan
[3] Univ New South Wales, Sch Mech & Mfg Engn, Sydney, NSW 2052, Australia
基金
英国医学研究理事会; 澳大利亚研究理事会;
关键词
Electrochemical sensor; Aptamer; Tetrahedral DNA nanostructure; Chronoamperometry; Thrombin; Continuous measurement; PROBE CARRIER PLATFORM; SMALL MOLECULES; NUCLEIC-ACIDS; APTASENSOR; BIOSENSOR; OPTIMIZATION; DENSITY;
D O I
10.1016/j.aca.2024.342587
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Tetrahedral DNA nanostructure (TDN) is highly promising in developing electrochemical aptamer-based (E -AB) sensors for biomolecular detection, owing to its inherit programmability, spatial orientation and structural robustness. However, current interrogation strategies applied for TDN-based E -AB sensors, including enzymebased amperometry, voltammetry, and electrochemical impedance spectroscopy, either require complicated probe design or suffer from limited applicability or selectivity. In this study, a TDN pendulum -empowered E -AB sensor interrogated by chronoamperometry for reagent -free and continuous monitoring of a blood clotting enzyme, thrombin, was developed. TDN pendulums with extended aptamer sequences at three vertices were immobilized on a gold electrode via a thiolated double -stranded DNA (dsDNA) at the fourth vertex, and their motion is modulated by the bonding of target thrombin to aptamers. We observed a significantly amplified signalling output on our sensor based on the TDN pendulum compared to E -AB sensors modified with linear pendulums. Moreover, our sensor achieved highly selective and rapidly responsive measurement of thrombin in both PBS and artificial urine, with a wide dynamic range from 1 pM to 10 nM. This study shows chronoamperometry-enabled continuous biomarker monitoring on a sub -second timescale with a drift -free baseline, demonstrating a novel approach to accurately detect molecular dynamics in real time.
引用
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页数:8
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