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Human dopamine receptor nanovesicles for gate-potential modulators in high-performance field-effect transistor biosensors

The development of molecular detection that allows rapid responses with high sensitivity and selectivity remains challenging. Herein, we demonstrate the strategy of novel bio-nanotechnology to successfully fabricate high-performance dopamine (DA) biosensor using DA Receptor-containing uniform-partic...

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Autores principales: Park, Seon Joo, Song, Hyun Seok, Kwon, Oh Seok, Chung, Ji Hyun, Lee, Seung Hwan, An, Ji Hyun, Ahn, Sae Ryun, Lee, Ji Eun, Yoon, Hyeonseok, Park, Tai Hyun, Jang, Jyongsik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3949245/
https://www.ncbi.nlm.nih.gov/pubmed/24614248
http://dx.doi.org/10.1038/srep04342
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author Park, Seon Joo
Song, Hyun Seok
Kwon, Oh Seok
Chung, Ji Hyun
Lee, Seung Hwan
An, Ji Hyun
Ahn, Sae Ryun
Lee, Ji Eun
Yoon, Hyeonseok
Park, Tai Hyun
Jang, Jyongsik
author_facet Park, Seon Joo
Song, Hyun Seok
Kwon, Oh Seok
Chung, Ji Hyun
Lee, Seung Hwan
An, Ji Hyun
Ahn, Sae Ryun
Lee, Ji Eun
Yoon, Hyeonseok
Park, Tai Hyun
Jang, Jyongsik
author_sort Park, Seon Joo
collection PubMed
description The development of molecular detection that allows rapid responses with high sensitivity and selectivity remains challenging. Herein, we demonstrate the strategy of novel bio-nanotechnology to successfully fabricate high-performance dopamine (DA) biosensor using DA Receptor-containing uniform-particle-shaped Nanovesicles-immobilized Carboxylated poly(3,4-ethylenedioxythiophene) (CPEDOT) NTs (DRNCNs). DA molecules are commonly associated with serious diseases, such as Parkinson's and Alzheimer's diseases. For the first time, nanovesicles containing a human DA receptor D1 (hDRD1) were successfully constructed from HEK-293 cells, stably expressing hDRD1. The nanovesicles containing hDRD1 as gate-potential modulator on the conducting polymer (CP) nanomaterial transistors provided high-performance responses to DA molecule owing to their uniform, monodispersive morphologies and outstanding discrimination ability. Specifically, the DRNCNs were integrated into a liquid-ion gated field-effect transistor (FET) system via immobilization and attachment processes, leading to high sensitivity and excellent selectivity toward DA in liquid state. Unprecedentedly, the minimum detectable level (MDL) from the field-induced DA responses was as low as 10 pM in real- time, which is 10 times more sensitive than that of previously reported CP based-DA biosensors. Moreover, the FET-type DRNCN biosensor had a rapid response time (<1 s) and showed excellent selectivity in human serum.
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spelling pubmed-39492452014-03-12 Human dopamine receptor nanovesicles for gate-potential modulators in high-performance field-effect transistor biosensors Park, Seon Joo Song, Hyun Seok Kwon, Oh Seok Chung, Ji Hyun Lee, Seung Hwan An, Ji Hyun Ahn, Sae Ryun Lee, Ji Eun Yoon, Hyeonseok Park, Tai Hyun Jang, Jyongsik Sci Rep Article The development of molecular detection that allows rapid responses with high sensitivity and selectivity remains challenging. Herein, we demonstrate the strategy of novel bio-nanotechnology to successfully fabricate high-performance dopamine (DA) biosensor using DA Receptor-containing uniform-particle-shaped Nanovesicles-immobilized Carboxylated poly(3,4-ethylenedioxythiophene) (CPEDOT) NTs (DRNCNs). DA molecules are commonly associated with serious diseases, such as Parkinson's and Alzheimer's diseases. For the first time, nanovesicles containing a human DA receptor D1 (hDRD1) were successfully constructed from HEK-293 cells, stably expressing hDRD1. The nanovesicles containing hDRD1 as gate-potential modulator on the conducting polymer (CP) nanomaterial transistors provided high-performance responses to DA molecule owing to their uniform, monodispersive morphologies and outstanding discrimination ability. Specifically, the DRNCNs were integrated into a liquid-ion gated field-effect transistor (FET) system via immobilization and attachment processes, leading to high sensitivity and excellent selectivity toward DA in liquid state. Unprecedentedly, the minimum detectable level (MDL) from the field-induced DA responses was as low as 10 pM in real- time, which is 10 times more sensitive than that of previously reported CP based-DA biosensors. Moreover, the FET-type DRNCN biosensor had a rapid response time (<1 s) and showed excellent selectivity in human serum. Nature Publishing Group 2014-03-11 /pmc/articles/PMC3949245/ /pubmed/24614248 http://dx.doi.org/10.1038/srep04342 Text en Copyright © 2014, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by-nc-sa/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/
spellingShingle Article
Park, Seon Joo
Song, Hyun Seok
Kwon, Oh Seok
Chung, Ji Hyun
Lee, Seung Hwan
An, Ji Hyun
Ahn, Sae Ryun
Lee, Ji Eun
Yoon, Hyeonseok
Park, Tai Hyun
Jang, Jyongsik
Human dopamine receptor nanovesicles for gate-potential modulators in high-performance field-effect transistor biosensors
title Human dopamine receptor nanovesicles for gate-potential modulators in high-performance field-effect transistor biosensors
title_full Human dopamine receptor nanovesicles for gate-potential modulators in high-performance field-effect transistor biosensors
title_fullStr Human dopamine receptor nanovesicles for gate-potential modulators in high-performance field-effect transistor biosensors
title_full_unstemmed Human dopamine receptor nanovesicles for gate-potential modulators in high-performance field-effect transistor biosensors
title_short Human dopamine receptor nanovesicles for gate-potential modulators in high-performance field-effect transistor biosensors
title_sort human dopamine receptor nanovesicles for gate-potential modulators in high-performance field-effect transistor biosensors
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3949245/
https://www.ncbi.nlm.nih.gov/pubmed/24614248
http://dx.doi.org/10.1038/srep04342
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