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Triple-Helix Molecular Switch Electrochemical Ratiometric Biosensor for Ultrasensitive Detection of Nucleic Acids.

Authors :
Xiong E
Li Z
Zhang X
Zhou J
Yan X
Liu Y
Chen J
Source :
Analytical chemistry [Anal Chem] 2017 Sep 05; Vol. 89 (17), pp. 8830-8835. Date of Electronic Publication: 2017 Aug 21.
Publication Year :
2017

Abstract

Biomolecular receptors such as nucleic acids that switch between two or more conformations upon binding to a specific target can be used to build specific and sensitive biosensors. In this work, based on the electrochemical dual-signaling ratiometric strategy and triple-helix molecular switch, we developed a selective, reusable, and simple electrochemical DNA (E-DNA) biosensor for target DNA (T-DNA) detection. A hairpin DNA capture probe labeled with methylene blue (MB-DNA) self-assembles on the surface of a gold electrode (GE) through Au-S bond, and then a single-strand DNA modified with two ferrocenes (Fc-DNA) on each end to enhance the oxidation signal hybridizes with the MB-DNA to form a triple-helix conformation. When T-DNA exists, the Fc-DNA hybridizes with T-DNA disassembling the triple-helix stem and allowing the MB-DNA to revert to its hairpin structure. Hence, the Fc tags diffuse away from the GE surface while the MB tags remain affixed close to it, resulting in a decrease in the peak current of Fc (I <subscript>Fc</subscript> ) and an increase in that of MB (I <subscript>MB</subscript> ). The linear relationship between the value of I <subscript>MB</subscript> /I <subscript>Fc</subscript> and the T-DNA concentration is observed from 0.5 to 80 pM, and the limit of detection is as low as 0.12 pM. The developed E-DNA biosensor may have great potential in the electrochemical detection of a wide range of analytes and be a biosensing platform for early clinical diagnosis and biomedical research.

Details

Language :
English
ISSN :
1520-6882
Volume :
89
Issue :
17
Database :
MEDLINE
Journal :
Analytical chemistry
Publication Type :
Academic Journal
Accession number :
28805061
Full Text :
https://doi.org/10.1021/acs.analchem.7b01251