A novel graphene-DNA biosensor for selective detection of mercury ions

A novel electrochemical biosensor for sensitive and selective detection of mercury (II) ions (Hg2+) based on a DNA grafted graphene is proposed. Graphene oxide (GO) was reduced by dopamine, and then the single-strand probe DNA modified at the 5′-end with an alkylamino modifier (NH2-ssDNA) was grafte...

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Veröffentlicht in:Biosensors & bioelectronics 2013-10, Vol.48, p.180-187
Hauptverfasser: Zhang, Yang, Zhao, Hong, Wu, Zhijiao, Xue, Ying, Zhang, Xiaofang, He, Yujian, Li, Xiangjun, Yuan, Zhuobin
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container_end_page 187
container_issue
container_start_page 180
container_title Biosensors & bioelectronics
container_volume 48
creator Zhang, Yang
Zhao, Hong
Wu, Zhijiao
Xue, Ying
Zhang, Xiaofang
He, Yujian
Li, Xiangjun
Yuan, Zhuobin
description A novel electrochemical biosensor for sensitive and selective detection of mercury (II) ions (Hg2+) based on a DNA grafted graphene is proposed. Graphene oxide (GO) was reduced by dopamine, and then the single-strand probe DNA modified at the 5′-end with an alkylamino modifier (NH2-ssDNA) was grafted on the reduced graphene oxide (RGO) surface via Michael addition reaction. In the presence of Hg2+, the target DNA with four thymine–thymine (T–T) mismatches would hybridize with the probe DNA on the glassy carbon electrode (GCE) through T–Hg2+–T coordination chemistry. The hybridization of the two oligonucleotides leads to the increase in the peak currents of [Ru(NH3)6]3+, which could be used for electrochemical sensing of Hg2+. The difference in the value of the peak currents of [Ru(NH3)6]3+ before and after DNA hybridization was linear with the concentration of Hg2+ in the range from 8.0×10−9 to 1.0×10−7M with a linear coefficiency of 0.996. The detection limit was 5.0×10−9M (S/N=3). The proposed electrochemical biosensor is rapid, convenient and low-cost for effective sensing of Hg2+. Particularly, the proposed method was applied successfully to the determination of Hg2+ in real environmental samples. •A novel graphene biosensor for Hg2+ based on T–Hg2+–T structure is realized.•The single-strand DNA was grafted on the RGO surface via Michael addition reaction.•A detection limit of 5.0×10−9M Hg2+ was obtained (S/N=3).•The proposed method was used to analyze Hg2+ in river water.
doi_str_mv 10.1016/j.bios.2013.04.013
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Graphene oxide (GO) was reduced by dopamine, and then the single-strand probe DNA modified at the 5′-end with an alkylamino modifier (NH2-ssDNA) was grafted on the reduced graphene oxide (RGO) surface via Michael addition reaction. In the presence of Hg2+, the target DNA with four thymine–thymine (T–T) mismatches would hybridize with the probe DNA on the glassy carbon electrode (GCE) through T–Hg2+–T coordination chemistry. The hybridization of the two oligonucleotides leads to the increase in the peak currents of [Ru(NH3)6]3+, which could be used for electrochemical sensing of Hg2+. The difference in the value of the peak currents of [Ru(NH3)6]3+ before and after DNA hybridization was linear with the concentration of Hg2+ in the range from 8.0×10−9 to 1.0×10−7M with a linear coefficiency of 0.996. The detection limit was 5.0×10−9M (S/N=3). The proposed electrochemical biosensor is rapid, convenient and low-cost for effective sensing of Hg2+. Particularly, the proposed method was applied successfully to the determination of Hg2+ in real environmental samples. •A novel graphene biosensor for Hg2+ based on T–Hg2+–T structure is realized.•The single-strand DNA was grafted on the RGO surface via Michael addition reaction.•A detection limit of 5.0×10−9M Hg2+ was obtained (S/N=3).•The proposed method was used to analyze Hg2+ in river water.</description><identifier>ISSN: 0956-5663</identifier><identifier>EISSN: 1873-4235</identifier><identifier>DOI: 10.1016/j.bios.2013.04.013</identifier><identifier>PMID: 23685314</identifier><language>eng</language><publisher>Kidlington: Elsevier B.V</publisher><subject>Biological and medical sciences ; Biosensing Techniques - methods ; Biosensor ; Biosensors ; Biotechnology ; Cations, Divalent - analysis ; DNA - chemistry ; Electrochemical Techniques - methods ; Fundamental and applied biological sciences. 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Graphene oxide (GO) was reduced by dopamine, and then the single-strand probe DNA modified at the 5′-end with an alkylamino modifier (NH2-ssDNA) was grafted on the reduced graphene oxide (RGO) surface via Michael addition reaction. In the presence of Hg2+, the target DNA with four thymine–thymine (T–T) mismatches would hybridize with the probe DNA on the glassy carbon electrode (GCE) through T–Hg2+–T coordination chemistry. The hybridization of the two oligonucleotides leads to the increase in the peak currents of [Ru(NH3)6]3+, which could be used for electrochemical sensing of Hg2+. The difference in the value of the peak currents of [Ru(NH3)6]3+ before and after DNA hybridization was linear with the concentration of Hg2+ in the range from 8.0×10−9 to 1.0×10−7M with a linear coefficiency of 0.996. The detection limit was 5.0×10−9M (S/N=3). The proposed electrochemical biosensor is rapid, convenient and low-cost for effective sensing of Hg2+. Particularly, the proposed method was applied successfully to the determination of Hg2+ in real environmental samples. •A novel graphene biosensor for Hg2+ based on T–Hg2+–T structure is realized.•The single-strand DNA was grafted on the RGO surface via Michael addition reaction.•A detection limit of 5.0×10−9M Hg2+ was obtained (S/N=3).•The proposed method was used to analyze Hg2+ in river water.</description><subject>Biological and medical sciences</subject><subject>Biosensing Techniques - methods</subject><subject>Biosensor</subject><subject>Biosensors</subject><subject>Biotechnology</subject><subject>Cations, Divalent - analysis</subject><subject>DNA - chemistry</subject><subject>Electrochemical Techniques - methods</subject><subject>Fundamental and applied biological sciences. 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Graphene oxide (GO) was reduced by dopamine, and then the single-strand probe DNA modified at the 5′-end with an alkylamino modifier (NH2-ssDNA) was grafted on the reduced graphene oxide (RGO) surface via Michael addition reaction. In the presence of Hg2+, the target DNA with four thymine–thymine (T–T) mismatches would hybridize with the probe DNA on the glassy carbon electrode (GCE) through T–Hg2+–T coordination chemistry. The hybridization of the two oligonucleotides leads to the increase in the peak currents of [Ru(NH3)6]3+, which could be used for electrochemical sensing of Hg2+. The difference in the value of the peak currents of [Ru(NH3)6]3+ before and after DNA hybridization was linear with the concentration of Hg2+ in the range from 8.0×10−9 to 1.0×10−7M with a linear coefficiency of 0.996. The detection limit was 5.0×10−9M (S/N=3). The proposed electrochemical biosensor is rapid, convenient and low-cost for effective sensing of Hg2+. 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subjects Biological and medical sciences
Biosensing Techniques - methods
Biosensor
Biosensors
Biotechnology
Cations, Divalent - analysis
DNA - chemistry
Electrochemical Techniques - methods
Fundamental and applied biological sciences. Psychology
Graphene
Graphite - chemistry
Limit of Detection
Mercury - analysis
Mercury ions
Methods. Procedures. Technologies
Michael addition
Nucleic acids
Rivers - chemistry
Various methods and equipments
title A novel graphene-DNA biosensor for selective detection of mercury ions
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