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DNA probe modified with 3-iron bis(dicarbollide) for electrochemical determination of DNA sequence of Avian Influenza Virus H5N1.

Grabowska, Iwona and Stachyra, Anna and Góra-Sochacka, Anna and Sirko, Agnieszka and Olejniczak, Agnieszka B and Leśnikowski, Zbigniew J and Radecki, Jerzy and Radecka, Hanna (2014) DNA probe modified with 3-iron bis(dicarbollide) for electrochemical determination of DNA sequence of Avian Influenza Virus H5N1. Biosensors & bioelectronics, 51 . pp. 170-6. ISSN 1873-4235

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Official URL: http://www.sciencedirect.com/science/article/pii/S...

Abstract

In this work, we report on oligonucleotide probes bearing metallacarborane [3-iron bis(dicarbollide)] redox label, deposited on gold electrode for electrochemical determination of DNA sequence derived from Avian Influenza Virus (AIV), type H5N1. The oligonucleotide probes containing 5'-terminal NH2 group were covalently attached to the electrode, via NHS/EDC coupling to 3-mercaptopropionic acid SAM, previously deposited on the surface of gold. The changes in redox activity of Fe(III) centre of the metallacarborane complex before and after hybridization process was used as analytical signal. The signals generated upon hybridization with targets such as complementary or non-complementary 20-mer ssDNA or various PCR products consisting of 180-190 bp (dsDNA) were recorded by Osteryoung square-wave voltammetry (OSWV). The developed system was very sensitive towards targets containing sequence complementary to the probe with the detection limit estimated as 0.03 fM (S/N=3.0) and 0.08 fM (S/N=3.0) for 20-mer ssDNA and for dsDNA (PCR product), respectively. The non-complementary targets generated very weak responses. Furthermore, the proposed genosensor was suitable for discrimination of PCR products with different location of the complementarity region.

Item Type:Article
Subjects:Q Science > QD Chemistry
Q Science > QR Microbiology > QR355 Virology
T Technology > TP Chemical technology
ID Code:764
Deposited By: dr Anna Gora-Sochacka
Deposited On:31 Oct 2014 08:58
Last Modified:31 Oct 2014 08:58

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