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Development of An Impedimetric Aptasensor for the Detection of Staphylococcus aureus
In combination with electrochemical impedance spectroscopy, aptamer-based biosensors are a powerful tool for fast analytical devices. Herein, we present an impedimetric aptasensor for the detection of the human pathogen Staphylococcus aureus. The used aptamer targets protein A, a surface bound virul...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5713450/ https://www.ncbi.nlm.nih.gov/pubmed/29160851 http://dx.doi.org/10.3390/ijms18112484 |
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author | Reich, Peggy Stoltenburg, Regina Strehlitz, Beate Frense, Dieter Beckmann, Dieter |
author_facet | Reich, Peggy Stoltenburg, Regina Strehlitz, Beate Frense, Dieter Beckmann, Dieter |
author_sort | Reich, Peggy |
collection | PubMed |
description | In combination with electrochemical impedance spectroscopy, aptamer-based biosensors are a powerful tool for fast analytical devices. Herein, we present an impedimetric aptasensor for the detection of the human pathogen Staphylococcus aureus. The used aptamer targets protein A, a surface bound virulence factor of S. aureus. The thiol-modified protein A-binding aptamer was co-immobilized with 6-mercapto-1-hexanol onto gold electrodes by self-assembly. Optimization of the ratio of aptamer to 6-mercapto-1-hexanol resulted in an average density of 1.01 ± 0.44 × 10(13) aptamer molecules per cm(2). As shown with quartz crystal microbalance experiments, the immobilized aptamer retained its functionality to bind recombinant protein A. Our impedimetric biosensor is based on the principle that binding of target molecules to the immobilized aptamer decreases the electron transfer between electrode and ferri-/ferrocyanide in solution, which is measured as an increase of impedance. Microscale thermophoresis measurements showed that addition of the redox probe ferri-/ferrocyanide has no influence on the binding of aptamer and its target. We demonstrated that upon incubation with various concentrations of S. aureus, the charge-transfer resistance increased proportionally. The developed biosensor showed a limit of detection of 10 CFU·mL(−1) and results were available within 10 minutes. The biosensor is highly selective, distinguishing non-target bacteria such as Escherichia coli and Staphylococcus epidermidis. This work highlights the immense potential of impedimetric aptasensors for future biosensing applications. |
format | Online Article Text |
id | pubmed-5713450 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-57134502017-12-07 Development of An Impedimetric Aptasensor for the Detection of Staphylococcus aureus Reich, Peggy Stoltenburg, Regina Strehlitz, Beate Frense, Dieter Beckmann, Dieter Int J Mol Sci Article In combination with electrochemical impedance spectroscopy, aptamer-based biosensors are a powerful tool for fast analytical devices. Herein, we present an impedimetric aptasensor for the detection of the human pathogen Staphylococcus aureus. The used aptamer targets protein A, a surface bound virulence factor of S. aureus. The thiol-modified protein A-binding aptamer was co-immobilized with 6-mercapto-1-hexanol onto gold electrodes by self-assembly. Optimization of the ratio of aptamer to 6-mercapto-1-hexanol resulted in an average density of 1.01 ± 0.44 × 10(13) aptamer molecules per cm(2). As shown with quartz crystal microbalance experiments, the immobilized aptamer retained its functionality to bind recombinant protein A. Our impedimetric biosensor is based on the principle that binding of target molecules to the immobilized aptamer decreases the electron transfer between electrode and ferri-/ferrocyanide in solution, which is measured as an increase of impedance. Microscale thermophoresis measurements showed that addition of the redox probe ferri-/ferrocyanide has no influence on the binding of aptamer and its target. We demonstrated that upon incubation with various concentrations of S. aureus, the charge-transfer resistance increased proportionally. The developed biosensor showed a limit of detection of 10 CFU·mL(−1) and results were available within 10 minutes. The biosensor is highly selective, distinguishing non-target bacteria such as Escherichia coli and Staphylococcus epidermidis. This work highlights the immense potential of impedimetric aptasensors for future biosensing applications. MDPI 2017-11-21 /pmc/articles/PMC5713450/ /pubmed/29160851 http://dx.doi.org/10.3390/ijms18112484 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Reich, Peggy Stoltenburg, Regina Strehlitz, Beate Frense, Dieter Beckmann, Dieter Development of An Impedimetric Aptasensor for the Detection of Staphylococcus aureus |
title | Development of An Impedimetric Aptasensor for the Detection of Staphylococcus aureus |
title_full | Development of An Impedimetric Aptasensor for the Detection of Staphylococcus aureus |
title_fullStr | Development of An Impedimetric Aptasensor for the Detection of Staphylococcus aureus |
title_full_unstemmed | Development of An Impedimetric Aptasensor for the Detection of Staphylococcus aureus |
title_short | Development of An Impedimetric Aptasensor for the Detection of Staphylococcus aureus |
title_sort | development of an impedimetric aptasensor for the detection of staphylococcus aureus |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5713450/ https://www.ncbi.nlm.nih.gov/pubmed/29160851 http://dx.doi.org/10.3390/ijms18112484 |
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