Electrogenerated chemiluminescence resonance energy transfer between luminol and MnO2 nanosheets decorated with Cu2O nanoparticles for sensitive detection of RNase H

被引:3
|
作者
Shi, Yahao [1 ]
Chen, Chunting [1 ]
Zhang, Yahui [1 ]
Dong, Yongping [1 ]
Wang, Shangbing [1 ]
机构
[1] Anhui Univ Technol, Inst Engn, Sch Chem & Chem Engn, Maanshan 243002, Anhui, Peoples R China
基金
中国国家自然科学基金;
关键词
GRAPHENE OXIDE; RIBONUCLEASE-H; HIGH-PERFORMANCE; QUANTUM DOTS; LABEL-FREE; ENZYME; ASSAY; DNA;
D O I
10.1039/d3an00002h
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
In the present work, a novel approach was developed for the preparation of Cu2O nanoparticle decorated MnO2 nanosheets (Cu2O@MnO2). Uniformly dispersed Cu2O nanocrystals were produced on the surface of MnO2 nanosheets by in situ reduction under refluxing conditions. The unique structure of the used MnO2 nanosheet support played a vital role in the preparation of such Cu2O@MnO2 nanocomposites. The electrogenerated chemiluminescence (ECL) resonance energy transfer can occur between the luminol/H2O2 system and Cu2O@MnO2 nanocomposites, resulting in a decrease of the ECL intensity, which can be used to fabricate an ECL sensor. Cu2O@MnO2 nanocomposite modified heterologous DNA/RNA duplexes were modified on the GCE to construct an ECL-RET system, leading to the decrease of ECL intensity. As a highly conserved damage repair protein, RNase H can specifically hydrolyze RNA in DNA/RNA strands to release Cu2O@MnO2 nanocomposites and recover the ECL signal. As a result, an "off-on" mode ECL sensor for sensitive RNase H assay was fabricated. Under the optimal conditions, the detection limit of RNase H is 0.0005 U mL(-1), which is superior to other approaches. The proposed method provides a universal platform for monitoring RNase H, and exhibits great potential in bioanalysis.
引用
收藏
页码:1300 / 1308
页数:9
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