CdTe nanocrystal-based electrochemical biosensor for the recognition of neutravidin by anodic stripping voltammetry at electrodeposited bismuth film

被引:31
作者
Du, Dan [1 ]
Ding, Jiawang [1 ]
Tao, Yuan [1 ]
Li, Haibing [1 ]
Chen, Xi [2 ]
机构
[1] Cent China Normal Univ, Minist Educ, Key Lab Pesticide &Chem Biol, Wuhan 430079, Peoples R China
[2] Xiamen Univ, Dept Chem, State Key Lab Marine Environm Sci, Xiamen 361005, Peoples R China
基金
中国国家自然科学基金; 高等学校博士学科点专项科研基金;
关键词
Biosensor; CdTe quantum dots; Anodic stripping voltammetry; Electrodeposition; Bismuth film; Neutravidin;
D O I
10.1016/j.bios.2008.07.020
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
CdTe quantum dots (QDs)-based electrochemical sensor for recognition of neutravidin, as a model protein, using anodic stripping voltammetry at electrodeposited bismuth film is presented. This biosensor involves the immobilization of the captured QDs conjugates which was dissolved with 1 M HCl solution to release cadmium ions and metal components were quantified by anodic stripping voltammetry after a 3-min accumulation at -1.2 V on bismuth-film electrode (BiFE) of the biotin, served as recognition element, onto the gold surface in connection with a cysteamine self-assembled monolayer. The modification procedure was characterized by electrochemical impedance spectroscopy and atomic force microscopy. We exploit QDs as labels for amplifying signal output and monitoring the extent of competition process between CdTe-labeled neutravidin and the target neutravidin for the limited binding sites on biotin. As expected for the competitive mechanism, the recognition event thus yields distinct cadmium stripping voltammetric current peak, whose response decreases upon increasing the level of target neutravidin concentrations. Under optimal conditions, the voltammetric response is highly linear over the range of 0.5-100 ng L(-1) neutravidin and the limit of detection is estimated to be 0.3 ng L(-1) (5 nM). Unlike earlier two-step sandwich bioassays, the present protocol relies on a one-step competitive assay, which is more accurate and sensitive, showing great promise for rapid, simple and cost-effective analysis of protein. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:863 / 868
页数:6
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