A hairpin aptamer-based electrochemical biosensing platform for the sensitive detection of proteins

被引:64
作者
Wu, Zai-Sheng [1 ]
Zheng, Fan [1 ]
Shen, Guo-Li [1 ]
Yu, Ru-Qin [1 ]
机构
[1] Hunan Univ, Coll Chem & Chem Engn, State Key Lab Chemo Biosensing & Chemometr, Changsha, Peoples R China
基金
中国国家自然科学基金;
关键词
Aptamer probe; Conformational change; Electron-transfer distance; Alternating current voltammetry; SWITCHING SIGNALING APTAMERS; DNA APTAMER; FLUORESCENCE ANISOTROPY; BIOLOGICAL-FLUIDS; REAGENTLESS; SENSORS; IGE; HYBRIDIZATION; APTASENSOR; LIGANDS;
D O I
10.1016/j.biomaterials.2009.02.017
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
An aptamer-based electrochemical sensing platform for the direct protein detection has been developed using IgE and a specifically designed aptamer with hairpin structure as the model analyte and probe sequence, respectively. In the absence of IgE, the aptamer immobilized on an electrode surface forms a large hairpin due to the hybridization of the two complementary arm sequences, and peak currents of redox species dissolved in solution can be achieved. However, the target protein binding can not only cause the increase of the dielectric layer but also trigger the significant conformational switching of the aptamer due to the opening of the designed hairpin structure that pushes the biomolecule layer/electrolyte interface away from the electrode surface, suppressing substantially the electron transfer (eT) and resulting in a strong detection signal. The detection limit of 3.6 x 10(-11) M and linear response range of 5.4 x 10(-11) to 3.6 x 10(-8) M are achieved without any amplifier. The selectivity is confirmed by interference test. More importantly, an innovative concept of adapting intelligently a surface-con fined aptamer sequence is introduced, and the limitations of the conventional electrochemical aptasensors have been overcome. The proposed sensing scheme is expected to become a promising strategy for the detection of proteins and other biomacromolecules. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2950 / 2955
页数:6
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