Electrochemical detection of osmium tetroxide-labeled PCR-products by means of protective strands

被引:29
作者
Reske, Thomas [1 ]
Mix, Maren [1 ,2 ]
Bahl, Hubert [2 ]
Flechsig, Gerd-Uwe [1 ]
机构
[1] Univ Rostock, Dept Chem, D-18051 Rostock, Germany
[2] Univ Rostock, Dept Biol Sci, D-18051 Rostock, Germany
关键词
PCR product; protective strand; osmium tetroxide bipyridine; gold electrode; probe SAM; DNA hybridization;
D O I
10.1016/j.talanta.2007.09.004
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
This communication reports about how single-stranded 136 base polymerase chain reaction (PCR) products labeled with electrochemically active osmium tetroxide bipyridine can be detected voltammetrically by hybridization with probe strands immobilized on gold electrodes. These electroactive ssDNA targets have been obtained by means of Lambda Exonuclease treatment of the double-stranded PCR products followed by hybridization of the remaining single strands with short protective strands and covalent labeling with osmium tetroxide bipyridine. Square-wave voltammetric signals of these osmium labels have been obtained only upon hybridization with the immobilized probe strands. An optimal 50 degrees C hybridization temperature has been found with a saturation of the probe layer at 30 min hybridization time and 7.5 nmol/l target concentration. The blank capture probe layer alone did not yield any signal. Unprotected strands produced almost no interference. Such double-selective switch-on electrochemical hybridization assays hold great promise for the specific detection of PCR products. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:393 / 397
页数:5
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