Electrochemical investigation of DNA-modified surfaces: From quantitation methods to experimental conditions

被引:47
作者
Ge, Bixia
Huang, Yu-Chuan
Sen, Dipankar
Yu, Hua-Zhong [1 ]
机构
[1] Simon Fraser Univ, Dept Chem, Burnaby, BC V5A 1S6, Canada
[2] Simon Fraser Univ, Dept Mol Biol & Biochem, Burnaby, BC V5A 1S6, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
DNA; self-assembled monolayers; gold; cyclic voltammetry; chronocoulometry;
D O I
10.1016/j.jelechem.2006.12.008
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
We have thoroughly compared cyclic voltammetry and chronocoulometry, the two commonly used electrochemical techniques in quantitative determination of DNA surface density on gold electrodes. The electrostatic binding of redox cations, such as [Ru(NH3)(6)](3+), to the anionic DNA phosphate backbone allows the determination of the number of phosphate residues and thereby the surface density of the oligonucleotide strands. The results obtained by the two methods agreed well with each other for thiol-terminated DNA immobilized on gold electrodes via Au-S linkages and for unmodified DNA physically adsorbed on the surface. An improved procedure has been developed for the preparation of DNA-modified gold chips with a relatively high surface coverage. The density of thiol-terminated single-stranded DNA probes was determined to be (2.2 +/- 0.3) x 10(13) molecules/cm(2) upon reaching adsorption equilibrium, which was in good agreement with that obtained by phosphor imaging of P-32-radiolabeled DNA. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:156 / 162
页数:7
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