Highly Sensitive Detection of Protein with Aptamer-Based Target-Triggering Two-Stage Amplification

被引:133
|
作者
Zhang, Zhen-zhu [1 ]
Zhang, Chun-yang [1 ]
机构
[1] Chinese Acad Sci, Shenzhen Inst Adv Technol, Single Mol Detect & Imaging Lab, Shenzhen 518055, Peoples R China
基金
中国国家自然科学基金;
关键词
ROLLING CIRCLE AMPLIFICATION; ISOTHERMAL DNA AMPLIFICATION; SIMIAN SARCOMA-VIRUS; SINGLE-STRANDED-DNA; GROWTH-FACTOR; CAPILLARY-ELECTROPHORESIS; ELECTROCHEMICAL DETECTION; CATALYTIC LABELS; POLYMERASE; LIGANDS;
D O I
10.1021/ac2029002
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Highly sensitive detection of proteins is essential to biomedical research as well as clinical diagnosis. However, so far most detection methods rely on antibody-based assays and are usually laborious and time-consuming with poor sensitivity. Here, we develop a simple and sensitive method for the detection of a biomarker protein, platelet-derived growth factor BB (PDGF-BB), based on aptamer-based target-triggering two-stage amplification. With the involvement of an aptamer-based probe and an exponential amplification reaction (EXPAR) template, our method combines strand displacement amplification (SDA) and EXPAR, transforming the probe conformational change induced by target binding into two-stage amplification and distinct fluorescence signal. This detection method exhibits excellent specificity and high sensitivity with a detection limit of 9.04 X 10(-13) M and a detection range of more than 5 orders of magnitude, which is comparable with or even superior to most currently used approaches for PDGF-BB detection. Moreover, this detection method has significant advantages of isothermal conditions required, simple and rapid without multiple separation and washing steps, low-cost without the need of any labeled DNA probes. Furthermore, this method might be extended to sensitive detection of a variety of biomolecules whose aptamers undergo similar conformational changes.
引用
收藏
页码:1623 / 1629
页数:7
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