Paper-based electrochemiluminescence origami device for protein detection using assembled cascade DNA-carbon dots nanotags based on rolling circle amplification

被引:70
作者
Wu, Ludan [1 ]
Ma, Chao [1 ]
Zheng, Xiaoxiao [1 ]
Liu, Haiyun [1 ]
Yu, Jinghua [1 ]
机构
[1] Univ Jinan, Key Lab Chem Sensing & Anal Univ Shandong, Sch Chem & Chem Engn, Jinan 250022, Peoples R China
基金
中国国家自然科学基金;
关键词
Lab-on-paper; Rolling circle amplification; H-IgG; Electrochemiluminescence; Carbon dots; LAB-ON-PAPER; ULTRASENSITIVE DETECTION; SIGNAL AMPLIFICATION; PLATFORM; IMMUNOSENSOR; IMMUNOASSAY; SENSORS;
D O I
10.1016/j.bios.2015.01.034
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
In this work, we developed a cascade signal amplification strategy for detection of IgG antigen by combining the rolling circle amplification (RCA) technique with oligonucleotide functionalized carbon dots (CDs), based on a paper-based electrochemiluminescence (ECL) origami device (PECLOD) for the first time. In this PECLOD, three-dimensional (3D) macroporous Au-paper electrode was fabricated and employed as the working electrode for specific and efficient antibodies capture. The RCA product containing tandem-repeat sequences could serve as an excellent template for periodic assembly of CDs, which presented per protein recognition event to numerous CDs tags for ECL readout. Under the optimal conditions, the proposed strategy showed remarkable amplification efficiency, very little nonspecific adsorption with good stability, reproducibility, and accuracy. Using human IgG (H-IgG) as a model protein, the designed strategy was successfully demonstrated for the ultrasensitive detection of protein target. The results revealed that the strategy exhibited a dynamic response to H-IgG range from 1.0 fM to 25 pM with a limit of detection as low as 0.15 fM. Importantly, the methodology can be further extended to the detection of other proteins or biomarkers. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:413 / 420
页数:8
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