Proximity-dependent protein detection based on enzyme-assisted fluorescence signal amplification

被引:36
|
作者
Tan, Yuyu [1 ]
Guo, Qiuping [1 ]
Zhao, Xiayu [1 ]
Yang, Xiaohai [1 ]
Wang, Kemin [1 ]
Huang, Jin [1 ]
Zhou, Yu [1 ]
机构
[1] Hunan Univ, State Key Lab ChemoBiosensing & Chemometr, Key Lab Bionanotechnol & Mol Engn Hunan Prov, Coll Biol,Coll Chem & Chem Engn, Changsha 410082, Hunan, Peoples R China
来源
基金
中国国家自然科学基金; 对外科技合作项目(国际科技项目);
关键词
Proximity effect; Enzyme-assisted signal amplification; Protein detection; ROLLING CIRCLE AMPLIFICATION; RESONANCE ENERGY-TRANSFER; NUCLEIC-ACID; ULTRASENSITIVE DETECTION; GOLD NANOPARTICLES; ALZHEIMERS-DISEASE; LIGATION ASSAYS; SMALL MOLECULES; HYBRIDIZATION; APTAMERS;
D O I
10.1016/j.bios.2013.08.001
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
In this paper, we develop a sensitive fluorescence method for protein detection based on proximity extension and enzyme-assisted signal amplification. In this novel method, pairs of proximity probes are designed, and the recognition elements are integrated into the proximity probes. Then proteins are detected by transforming aptamer or antibody-protein binding signals into DNA detection based on proximity effect. In addition, nick sites are introduced into the proximity probes to amplify the detectable signal. As proof of concept, detection of human a-thrombin and human IgG are demonstrated in this study. The aptamers and antibodies are coupled in the proximity probes as recognition elements for human a-thrombin and human IgG respectively. In the presence of target protein, aptamer or antibody-protein binding signals are transformed into detectable signals by the proximity effect, and can be further amplified by enzyme-assisted strand displacement. The above mentioned strategies consequently bring the limit of detection (LOD) to as low as 1 pM for human a-thrombin and 6 pM for human IgG. Furthermore, this method might be extended to sensitive detection of other proteins by changing recognition elements of proximity probes. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:255 / 260
页数:6
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