Simultaneous detection of multiple DNA targets based on encoding metal ions

被引:16
|
作者
Zheng, Lichun [1 ]
Li, Xiaoyan [1 ]
Liu, Panpan [1 ]
Wu, Guofan [1 ]
Lu, Xiaoquan [1 ]
Liu, Xiuhui [1 ]
机构
[1] Northwest Normal Univ, Coll Chem & Chem Engn, Key Lab Bioelectrochem & Environm Anal Gansu Prov, Lanzhou 730070, Gansu, Peoples R China
来源
基金
中国国家自然科学基金;
关键词
DNA biosensors; Multiplex analysis; Metallothioneins; Metal ions; Stripping voltammetry; ANODIC-STRIPPING VOLTAMMETRY; ELECTROCHEMICAL DETECTION; QUANTUM DOTS; METALLOTHIONEINS; SPECTROSCOPY; ELECTRODES; SENSOR;
D O I
10.1016/j.bios.2013.09.008
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
We present a novel strategy for simultaneous electrochemical detection of multiple DNA targets based on the use of different encoding metal ions as tags. The principle of this scheme is that metal ions bound to metallothionein (MT) molecules can be released down after hybridization with DNA targets and then be detected by stripping voltammetry. The novel detection probes, ssDNA/MT conjugates, covered with different metal ions were synthesized for the first time, then three encoding metal ions (Zn2+, Cd2+, and Pb2+) were used to differentiate the signals of three virus DNA due to their well-defined anodic stripping peaks at -1.13 V (Zn), -0.78 V (Cd), and -0.52 V (Pb) at BiFE, respectively. The anodic peak currents increased linearly with the concentrations of DNA targets in the range from 0.1 nM to 10 nM with a detection limit of 33 pM. In addition, the one-base mismatched target was effectively discriminated from the complementary target. The described results demonstrated that this method possesses high sensitivity and selectivity for multi-target DNA assay and has great potential in applications for detection of even more targets in biological assays, particularly immunoassays. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:354 / 359
页数:6
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