Preparation of an electrochemical PNA biosensor for detection of target DNA sequence and single nucleotide mutation on p53 tumor suppressor gene corresponding oligonucleotide

被引:67
作者
Raoof, Jahan Bakhsh [1 ]
Ojani, Reza [1 ]
Golabi, Seyed Mandi [2 ]
Hamidi-Asl, Ezat [1 ]
Hejazi, Mohammad Saeid [3 ,4 ,5 ]
机构
[1] Univ Mazandran, Fac Chem, Dept Analyt Chem, Electroanalyt Chem Res Lab, Babol Sar, Iran
[2] Tabriz Univ Med Sci, Fac Pharm, Tabriz, Iran
[3] Tabriz Univ Med Sci, Drug Appl Res Ctr, Tabriz, Iran
[4] Tabriz Univ Med Sci, Pharmaceut Nanotechnol Res Ctr, Tabriz, Iran
[5] Tabriz Univ, Electroanalyt Chem Res Lab, Dept Analyt Chem, Fac Chem, Tabriz, Iran
来源
SENSORS AND ACTUATORS B-CHEMICAL | 2011年 / 157卷 / 01期
关键词
Peptide nucleic acid; Self-assembled monolayer; Methylene blue; p53; Oligonucleotide; PEPTIDE NUCLEIC-ACIDS; ASSEMBLED ALKANETHIOL MONOLAYER; HUMAN INTERLEUKINE-2 GENE; METHYLENE-BLUE; IMPEDANCE SPECTROSCOPY; HYBRIDIZATION; GOLD; INDICATOR; TRANSDUCTION; ELECTRODE;
D O I
10.1016/j.snb.2011.03.049
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Development of an electrochemical biosensor based on peptide nucleic acid (PNA) probe for detection of target DNA sequence and single nucleotide mutation in p53 tumor suppressor gene corresponding oligonucleotide using methylene blue (MB) as an electrochemical indicator is described. The interaction between MB and short sequence of p53, one of the most important tumor suppressor genes due to its dysfunction in the majority of human cancers, was studied by differential pulse voltarnmety (DPV). Probe modified electrode was prepared by self-assembled monolayer (SAM) formation of thiolated PNA molecules on the surface of gold electrode (GE). The hybridization of PNA probe with target DNA was performed in solution to form PNA-DNA hybrid on the surface of the GE. A significant increase in the reduction signal of MB was observed upon hybridization of the probe with the complementary DNA. The selectivity of the biosensor was studied using noncomplementary oligonucleotides. Furthermore, our results confirmed the ability of the sensor to detect single base mismatch in the sample oligonucleoticle. The influence of probe concentration on the effective discrimination against noncomplementary sequence and point mutation was also investigated. Diagnostic performance of the biosensor is described and the detection limit is found 6.82 x 10(-10) M. The electrochemical impedance spectroscopy was also employed to further investigate the sensor function. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:195 / 201
页数:7
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