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Chemically Functionalised Graphene FET Biosensor for the Label-free Sensing of Exosomes

A graphene field-effect transistor (gFET) was non-covalently functionalised with 1-pyrenebutyric acid N-hydroxysuccinimide ester and conjugated with anti-CD63 antibodies for the label-free detection of exosomes. Using a microfluidic channel, part of a graphene film was exposed to solution. The chang...

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Autores principales: Kwong Hong Tsang, Deana, Lieberthal, Tyler J., Watts, Clare, Dunlop, Iain E., Ramadan, Sami, del Rio Hernandez, Armando E., Klein, Norbert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6763426/
https://www.ncbi.nlm.nih.gov/pubmed/31558796
http://dx.doi.org/10.1038/s41598-019-50412-9
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author Kwong Hong Tsang, Deana
Lieberthal, Tyler J.
Watts, Clare
Dunlop, Iain E.
Ramadan, Sami
del Rio Hernandez, Armando E.
Klein, Norbert
author_facet Kwong Hong Tsang, Deana
Lieberthal, Tyler J.
Watts, Clare
Dunlop, Iain E.
Ramadan, Sami
del Rio Hernandez, Armando E.
Klein, Norbert
author_sort Kwong Hong Tsang, Deana
collection PubMed
description A graphene field-effect transistor (gFET) was non-covalently functionalised with 1-pyrenebutyric acid N-hydroxysuccinimide ester and conjugated with anti-CD63 antibodies for the label-free detection of exosomes. Using a microfluidic channel, part of a graphene film was exposed to solution. The change in electrical properties of the exposed graphene created an additional minimum alongside the original Dirac point in the drain-source current (I(ds)) - back-gate voltage (V(g)) curve. When phosphate buffered saline (PBS) was present in the channel, the additional minimum was present at a V(g) lower than the original Dirac point and shifted with time when exosomes were introduced into the channel. This shift of the minimum from the PBS reference point reached saturation after 30 minutes and was observed for multiple exosome concentrations. Upon conjugation with an isotype control, sensor response to the highest concentration of exosomes was negligible in comparison to that with anti-CD63 antibody, indicating that the functionalised gFET can specifically detect exosomes at least down to 0.1 μg/mL and is sensitive to concentration. Such a gFET biosensor has not been used before for exosome sensing and could be an effective tool for the liquid-biopsy detection of exosomes as biomarkers for early-stage identification of diseases such as cancer.
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spelling pubmed-67634262019-10-02 Chemically Functionalised Graphene FET Biosensor for the Label-free Sensing of Exosomes Kwong Hong Tsang, Deana Lieberthal, Tyler J. Watts, Clare Dunlop, Iain E. Ramadan, Sami del Rio Hernandez, Armando E. Klein, Norbert Sci Rep Article A graphene field-effect transistor (gFET) was non-covalently functionalised with 1-pyrenebutyric acid N-hydroxysuccinimide ester and conjugated with anti-CD63 antibodies for the label-free detection of exosomes. Using a microfluidic channel, part of a graphene film was exposed to solution. The change in electrical properties of the exposed graphene created an additional minimum alongside the original Dirac point in the drain-source current (I(ds)) - back-gate voltage (V(g)) curve. When phosphate buffered saline (PBS) was present in the channel, the additional minimum was present at a V(g) lower than the original Dirac point and shifted with time when exosomes were introduced into the channel. This shift of the minimum from the PBS reference point reached saturation after 30 minutes and was observed for multiple exosome concentrations. Upon conjugation with an isotype control, sensor response to the highest concentration of exosomes was negligible in comparison to that with anti-CD63 antibody, indicating that the functionalised gFET can specifically detect exosomes at least down to 0.1 μg/mL and is sensitive to concentration. Such a gFET biosensor has not been used before for exosome sensing and could be an effective tool for the liquid-biopsy detection of exosomes as biomarkers for early-stage identification of diseases such as cancer. Nature Publishing Group UK 2019-09-26 /pmc/articles/PMC6763426/ /pubmed/31558796 http://dx.doi.org/10.1038/s41598-019-50412-9 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Kwong Hong Tsang, Deana
Lieberthal, Tyler J.
Watts, Clare
Dunlop, Iain E.
Ramadan, Sami
del Rio Hernandez, Armando E.
Klein, Norbert
Chemically Functionalised Graphene FET Biosensor for the Label-free Sensing of Exosomes
title Chemically Functionalised Graphene FET Biosensor for the Label-free Sensing of Exosomes
title_full Chemically Functionalised Graphene FET Biosensor for the Label-free Sensing of Exosomes
title_fullStr Chemically Functionalised Graphene FET Biosensor for the Label-free Sensing of Exosomes
title_full_unstemmed Chemically Functionalised Graphene FET Biosensor for the Label-free Sensing of Exosomes
title_short Chemically Functionalised Graphene FET Biosensor for the Label-free Sensing of Exosomes
title_sort chemically functionalised graphene fet biosensor for the label-free sensing of exosomes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6763426/
https://www.ncbi.nlm.nih.gov/pubmed/31558796
http://dx.doi.org/10.1038/s41598-019-50412-9
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