Fabrication of Polymeric Ferrocene Nanoparticles for Electrochemical Aptasensing of Protein with Target-Catalyzed Hairpin Assembly

被引:32
|
作者
Chai, Hua [1 ,2 ]
Cheng, Wenbo [1 ,3 ]
Xu, Lei [4 ]
Gui, Huiqiang [4 ]
He, Jinlin [4 ]
Miao, Peng [1 ,2 ]
机构
[1] Chinese Acad Sci, Suzhou Inst Biomed Engn & Technol, Suzhou 215163, Peoples R China
[2] Jihua Lab, Foshan 528200, Peoples R China
[3] Tianjin Guokeyigong Sci & Technol Dev Co Ltd, Tianjin 300399, Peoples R China
[4] Soochow Univ, Jiangsu Key Lab Adv Funct Polymer Design & Applic, State & Local Joint Engn Lab Novel Funct Polymer, Coll Chem Chem Engn & Mat Sci, Suzhou 215123, Peoples R China
基金
中国国家自然科学基金;
关键词
ROLLING CIRCLE AMPLIFICATION; LABEL-FREE; GOLD NANOPARTICLES; THROMBIN DETECTION; ULTRASENSITIVE DETECTION; SANDWICH STRUCTURE; DNA; STRATEGY; MICRORNA; SYSTEM;
D O I
10.1021/acs.analchem.9b01673
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Herein we describe a novel isothermal and enzyme-free electrochemical aptasensor for protein detection via the employment of polymeric ferrocene nanoparticles (PFcNPs) and target-catalyzed hairpin assembly amplification. The synthesized PFcNPs not only load numerous Fc molecules for enhanced electrochemical output but also possess plenty of amino groups, which increase the water solubility and facilitate the conjugation with the aptamer toward the recognition of target protein. After the formation of an aptamer/protein complex, the conformation of the DNA probe changes, which further triggers hairpin assembly on top of DNA tetrahedral structures modified on the electrode interface. The process can be recycled, and multiple PFcNPs are localized on the electrode. Thus, an amplified electrochemical signal is able to be recorded, which is sufficient to achieve a demonstrated limit of detection as low as 67 fM. This developed aptasensor can also discriminate target protein from other interfering substances with a high selectivity. Furthermore, it has been successfully applied in diluted real blood serum samples. All of these features make the present methodology a promising candidate for ultratrace protein biosensors.
引用
收藏
页码:9940 / 9945
页数:6
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