Enzyme-free colorimetric detection of MicroRNA-21 using metal chelator as label for signal generation and amplification

被引:21
作者
Piao, Jiafang [1 ,2 ]
Zhao, Qian [1 ,2 ]
Zhou, Dianming [3 ,4 ]
Peng, Weipan [1 ,2 ]
Gao, Weichen [1 ,2 ]
Chen, Minghui [1 ,2 ]
Shu, Guiming [5 ]
Gong, Xiaoqun [1 ,2 ,4 ]
Chang, Jin [1 ,2 ]
机构
[1] Tianjin Univ, Sch Life Sci, Tianjin 300072, Peoples R China
[2] Tianjin Engn Ctr Micronano Biomat & Detect Treatm, Tianjin 300072, Peoples R China
[3] Tianjin Ctr Dis Control & Prevent, Dept Toxicol, Tianjin 30000, Peoples R China
[4] Hunan Univ, State Key Lab Chemo Biosensing & Chemometr, Changsha 410082, Hunan, Peoples R China
[5] Tianjin Third Cent Hosp, Tianjin Enterprises Key Lab Blood Perfus Technol, Tianjin Key Lab Artificial Cell, Artificial Cell Engn Technol Res Ctr,Publ Hlth Mi, Tianjin 300170, Peoples R China
基金
中国国家自然科学基金;
关键词
microRNA; EDTA center dot 2Na; Plasmonic signal; AuNPs; GOLD NANOPARTICLES; HYDROGEN-PEROXIDE; VISUAL DETECTION; EXPRESSION; RECOGNITION; MECHANISM;
D O I
10.1016/j.aca.2018.11.044
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
MicroRNAs (miRNAs) were reported to be potential tumor markers for early diagnosis of cancer. Due to its short sequence, low expression level and high susceptibility to degradation, the stable and sensitive detection method of miRNAs is arduous to establish. In this work, we designed a metal chelator (ethylenediamine tetraacetic acid disodium salt, EDTA center dot 2Na) labeled oligonucleotides as the plasmonic signal supraregulator probe to control the generation of gold nanoparticles (AuNPs). Based on another complementary oligonucleotides of target miRNA labeling SiO2 microparticles (SiO(2)MPs) as the detecting platform, EDTA center dot 2Na labeled oligonucleotide probes were immobilized on the SiO2 platform through the sandwich structure in the presence of target miRNA. The sandwich chelating device could further chelate Au3+ to regulate the generation of AuNPs, resulting in colorimetric signal to qualitatively and quantitatively detect the concentration of microRNA-21 (miR-21). The results indicate that the proposed metal chelator-labeled signal amplification method has outstanding sensitivity (LOD = 8.9 fM) and excellent stability, which will be benefit for the early accurate diagnosis of miRNAs. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:145 / 152
页数:8
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