A novel protein analytical method based on hybrid-aptamer and DNA-arrayed electrodes

被引：12

作者：

Wang, Jinli ^{[1
]}

Xu, Danke ^{[1
,2
]}

Chen, Hong-Yuan ^{[1
]}

机构：

[1] Nanjing Univ, Sch Chem & Chem Engn, Minist Educ, Key Lab Analyt Chem Life Sci, Nanjing 210093, Peoples R China

[2] Beijing Proteome Res Ctr, State Key Lab Prote, Beijing 102206, Peoples R China

来源：

ELECTROCHEMISTRY COMMUNICATIONS | 2009年 / 11卷 / 08期

关键词：

DNA array; DNA-directed immobilization of aptamer; Human immunoglobulin E; SURFACE-PLASMON RESONANCE; HUMAN IGE; IMMOBILIZATION; BIOSENSOR;

D O I：

10.1016/j.elecom.2009.06.013

中图分类号：

O646 [电化学、电解、磁化学];

学科分类号：

081704 ;

摘要：

A novel protein assay method based on a DNA array was developed, in which human immunoglobulin E (hIgE) and its DNA aptamer were used as an analytical model. The target protein hIgE was captured by the aptamer in homogeneous solution and then the resulting hIgE-aptamer complex was hybridized onto probes self-assembled on the DNA array. Measured by electrochemical impedance spectroscopy (EIS), the charge transfer resistance (Rct) of electrodes before and after hybridization was compared. To test the selectivity of the method, four different probes with one to three mismatched bases were immobilized on respective electrodes. The results showed that the complex could be hybridized and detected out on the electrodes modified with the fully complementary sequences. In addition, the DNA array could be employed to analyze multiple samples selectively with the matched aptamer. (C) 2009 Elsevier B.V. All rights reserved.

引用

收藏

页码：1627 / 1630

页数：4

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