Bio-nanogate controlled enzymatic reaction for virus sensing.
Identifieur interne : 000077 ( PubMed/Checkpoint ); précédent : 000076; suivant : 000078Bio-nanogate controlled enzymatic reaction for virus sensing.
Auteurs : Ronghui Wang [États-Unis] ; Lizhou Xu [République populaire de Chine] ; Yanbin Li [États-Unis]Source :
- Biosensors & bioelectronics [ 1873-4235 ] ; 2015.
Descripteurs français
- KwdFr :
- MESH :
- génétique : Sous-type H5N1 du virus de la grippe A.
- isolement et purification : Sous-type H5N1 du virus de la grippe A.
- virologie : Grippe chez les oiseaux.
- Animaux, Hémagglutination virale, Limite de détection, Oiseaux, Or, Techniques de biocapteur.
English descriptors
- KwdEn :
- MESH :
- chemical , chemistry : Gold.
- genetics : Influenza A Virus, H5N1 Subtype.
- isolation & purification : Influenza A Virus, H5N1 Subtype.
- virology : Influenza in Birds.
- Animals, Biosensing Techniques, Birds, Hemagglutination, Viral, Limit of Detection.
Abstract
The objective of this study was to develop an aptamer-based bifunctional bio-nanogate, which could selectively respond to target molecules, and control enzymatic reaction for electrochemical measurements. It was successfully applied for sensitive, selective, rapid, quantitative, and label-free detection of avian influenza viruses (AIV) H5N1. A nanoporous gold film with pore size of ~20 nm was prepared by a metallic corrosion method, and the purity was checked by energy-dispersive X-ray spectroscopy (EDS) study. To improve the performance of the bio-nanogate biosensor, its main analytical parameters were studied and optimized. We demonstrated that the developed bio-nanogate was capable of controlling enzymatic reaction for AIV H5N1 sensing within 1h with a detection limit of 2(-9)HAU (hemagglutination units). The enzymatic reaction was able to cause significant current change due to the presence of target AIV. A linear relationship was found in the virus titer range of 2(-10)-2(2)HAU. No interference was observed from non-target AIV subtypes such as H1N1, H2N2, H4N8 and H7N2. The developed approach could be adopted for sensing of other viruses.
DOI: 10.1016/j.bios.2014.08.071
PubMed: 25212377
Affiliations:
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<term>Hemagglutination, Viral</term>
<term>Influenza A Virus, H5N1 Subtype (genetics)</term>
<term>Influenza A Virus, H5N1 Subtype (isolation & purification)</term>
<term>Influenza in Birds (virology)</term>
<term>Limit of Detection</term>
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<keywords scheme="KwdFr" xml:lang="fr"><term>Animaux</term>
<term>Grippe chez les oiseaux (virologie)</term>
<term>Hémagglutination virale</term>
<term>Limite de détection</term>
<term>Oiseaux</term>
<term>Or ()</term>
<term>Sous-type H5N1 du virus de la grippe A (génétique)</term>
<term>Sous-type H5N1 du virus de la grippe A (isolement et purification)</term>
<term>Techniques de biocapteur</term>
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<term>Limit of Detection</term>
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<term>Hémagglutination virale</term>
<term>Limite de détection</term>
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<term>Or</term>
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<front><div type="abstract" xml:lang="en">The objective of this study was to develop an aptamer-based bifunctional bio-nanogate, which could selectively respond to target molecules, and control enzymatic reaction for electrochemical measurements. It was successfully applied for sensitive, selective, rapid, quantitative, and label-free detection of avian influenza viruses (AIV) H5N1. A nanoporous gold film with pore size of ~20 nm was prepared by a metallic corrosion method, and the purity was checked by energy-dispersive X-ray spectroscopy (EDS) study. To improve the performance of the bio-nanogate biosensor, its main analytical parameters were studied and optimized. We demonstrated that the developed bio-nanogate was capable of controlling enzymatic reaction for AIV H5N1 sensing within 1h with a detection limit of 2(-9)HAU (hemagglutination units). The enzymatic reaction was able to cause significant current change due to the presence of target AIV. A linear relationship was found in the virus titer range of 2(-10)-2(2)HAU. No interference was observed from non-target AIV subtypes such as H1N1, H2N2, H4N8 and H7N2. The developed approach could be adopted for sensing of other viruses.</div>
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<Abstract><AbstractText>The objective of this study was to develop an aptamer-based bifunctional bio-nanogate, which could selectively respond to target molecules, and control enzymatic reaction for electrochemical measurements. It was successfully applied for sensitive, selective, rapid, quantitative, and label-free detection of avian influenza viruses (AIV) H5N1. A nanoporous gold film with pore size of ~20 nm was prepared by a metallic corrosion method, and the purity was checked by energy-dispersive X-ray spectroscopy (EDS) study. To improve the performance of the bio-nanogate biosensor, its main analytical parameters were studied and optimized. We demonstrated that the developed bio-nanogate was capable of controlling enzymatic reaction for AIV H5N1 sensing within 1h with a detection limit of 2(-9)HAU (hemagglutination units). The enzymatic reaction was able to cause significant current change due to the presence of target AIV. A linear relationship was found in the virus titer range of 2(-10)-2(2)HAU. No interference was observed from non-target AIV subtypes such as H1N1, H2N2, H4N8 and H7N2. The developed approach could be adopted for sensing of other viruses.</AbstractText>
<CopyrightInformation>Copyright © 2014 Elsevier B.V. All rights reserved.</CopyrightInformation>
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