Colorimetric and electrochemical dual-signal detection of uracil-DNA glycosylase using functionalized pure DNA hydrogel on paper-based analytical devices

Wei Xue , Pan Jia , Yunping Wu , Pu Wang , Jiarong Shi , Yangyang Chang , Meng Liu
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引用次数: 1

Abstract

The development of simple and accurate detection of uracil-DNA glycosylase (UDG) is of great significance for early clinical diagnosis and biomedical research. Here, we on the first effort introduced the uracil bases into the rolling circle amplification (RCA) reaction to produce the functionalized pure DNA hydrogel (PDH) for UDG detection. During RCA process, methylene blue (MB) molecules as the indicators were encapsulated into PDH. The addition of UDG can remove the uracil bases of PDH to generate abasic sites, which are further cleaved with the assistance of apurinic/apyrimidinic endonuclease (APE), thus resulting in the dissociation of PDH to release blue MB. By combining with the paper analytical devices as the signal readout platform, a colorimetric and electrochemical dual-signal biosensor was constructed for convenient and accurate detection of UDG. The proposed MB@PDH-based dual-signal sensing system exhibited good selectivity and high sensitivity with a detection limit of 6.4 × 10−4 U/mL (electrochemical method). It was also demonstrated that this sensing system showed excellent performance in UDG inhibitor screening, thus providing great potential in UDG-related disease diagnosis and drug discovery.

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利用功能化纯DNA水凝胶在纸基分析装置上比色法和电化学双信号检测尿嘧啶-DNA糖基酶
尿嘧啶脱氧核糖核酸糖基化酶(UDG)检测方法的发展对早期临床诊断和生物医学研究具有重要意义。在这里,我们首次将尿嘧啶碱基引入滚环扩增(RCA)反应,以产生用于UDG检测的功能化纯DNA水凝胶(PDH)。在RCA过程中,亚甲基蓝(MB)分子作为指示剂被封装到PDH中。UDG的加入可以去除PDH的尿嘧啶碱基以产生碱基位点,这些碱基位点在无嘌呤/无嘧啶核酸内切酶(APE)的帮助下被进一步切割,从而导致PDH解离以释放蓝色MB。结合论文中的分析装置作为信号读出平台,构建了一种方便、准确检测UDG的比色电化学双信号生物传感器MB@PDH-based双信号传感系统具有良好的选择性和高灵敏度,检测限为6.4×10−4U/mL(电化学法)。该传感系统在UDG抑制剂筛选中表现出优异的性能,在UDG相关疾病诊断和药物发现方面具有巨大的潜力。
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