An ultrasensitive signal-on electrochemical aptasensor via target-induced conjunction of split aptamer fragments

被引:71
作者
Chen, Jinghua [1 ,2 ]
Zhang, Jing [1 ,3 ]
Li, Juan [1 ]
Yang, Huang-Hao [1 ]
Fu, Fengfu [1 ]
Chen, Guonan [1 ]
机构
[1] Fuzhou Univ, Dept Chem, MOE, Key Lab Anal & Detect Technol Food Safety, Fuzhou 350002, Peoples R China
[2] Fujian Med Univ, Fac Pharm, Dept Pharmaceut Anal, Fuzhou 350004, Peoples R China
[3] Fujian Coll Med Occupat & Technol, Dept Pharmaceut, Fuzhou 350101, Peoples R China
基金
美国国家科学基金会;
关键词
Electrochemical aptasensor; Split aptamer fragments; Signal-on; IMPEDANCE SPECTROSCOPY; HUMAN THROMBIN; DNA; GOLD; REAGENTLESS; MONOLAYERS; SENSOR; BIND; INTERROGATION; BIOSENSORS;
D O I
10.1016/j.bios.2009.09.015
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
In this paper, we introduced a signal-on electrochemical sensor based on target-induced split aptamer fragments conjunction. To construct the aptasensor, the sequence of the 15-base anti-thrombin DNA aptamer was split into two fragments. one of which was attached to a gold electrode via thiol self-assembled monolayer chemistry and the second of which was modified with the redox moiety ferrocene. Thrombin-induced association of the two fragments thus increased the concentration of ferrocene at the electrode surface, which could be readily monitored via voltammetry. The sensitivity of the proposed electrochemical aptasensor was investigated by differential pulse voltammogram. The results indicated that, in pH 7.1 Tris-HCl buffer solution, the peak current was linear with the concentration of thrombin in the range of 0.8-15 nM with a detection limit of 0.2 nM. The proposed aptasensor has the advantages of higher sensitivity and lower background current. Given the simplicity in design of the proposed electrochemical aptasensor, it is fairly easy to generalize this strategy to detect a spectrum of targets by splitting the aptamers into two suitable segments. Furthermore, this design could be also used to construct novel optical aptasensors. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:996 / 1000
页数:5
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