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Precise and selective sensing of DNA-DNA hybridization by graphene/Si-nanowires diode-type biosensors
Single-Si-nanowire (NW)-based DNA sensors have been recently developed, but their sensitivity is very limited because of high noise signals, originating from small source-drain current of the single Si NW. Here, we demonstrate that chemical-vapor-deposition-grown large-scale graphene/surface-modifie...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4989226/ https://www.ncbi.nlm.nih.gov/pubmed/27534818 http://dx.doi.org/10.1038/srep31984 |
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author | Kim, Jungkil Park, Shin-Young Kim, Sung Lee, Dae Hun Kim, Ju Hwan Kim, Jong Min Kang, Hee Han, Joong-Soo Park, Jun Woo Lee, Hosun Choi, Suk-Ho |
author_facet | Kim, Jungkil Park, Shin-Young Kim, Sung Lee, Dae Hun Kim, Ju Hwan Kim, Jong Min Kang, Hee Han, Joong-Soo Park, Jun Woo Lee, Hosun Choi, Suk-Ho |
author_sort | Kim, Jungkil |
collection | PubMed |
description | Single-Si-nanowire (NW)-based DNA sensors have been recently developed, but their sensitivity is very limited because of high noise signals, originating from small source-drain current of the single Si NW. Here, we demonstrate that chemical-vapor-deposition-grown large-scale graphene/surface-modified vertical-Si-NW-arrays junctions can be utilized as diode-type biosensors for highly-sensitive and -selective detection of specific oligonucleotides. For this, a twenty-seven-base-long synthetic oligonucleotide, which is a fragment of human DENND2D promoter sequence, is first decorated as a probe on the surface of vertical Si-NW arrays, and then the complementary oligonucleotide is hybridized to the probe. This hybridization gives rise to a doping effect on the surface of Si NWs, resulting in the increase of the current in the biosensor. The current of the biosensor increases from 19 to 120% as the concentration of the target DNA varies from 0.1 to 500 nM. In contrast, such biosensing does not come into play by the use of the oligonucleotide with incompatible or mismatched sequences. Similar results are observed from photoluminescence microscopic images and spectra. The biosensors show very-uniform current changes with standard deviations ranging ~1 to ~10% by ten-times endurance tests. These results are very promising for their applications in accurate, selective, and stable biosensing. |
format | Online Article Text |
id | pubmed-4989226 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-49892262016-08-30 Precise and selective sensing of DNA-DNA hybridization by graphene/Si-nanowires diode-type biosensors Kim, Jungkil Park, Shin-Young Kim, Sung Lee, Dae Hun Kim, Ju Hwan Kim, Jong Min Kang, Hee Han, Joong-Soo Park, Jun Woo Lee, Hosun Choi, Suk-Ho Sci Rep Article Single-Si-nanowire (NW)-based DNA sensors have been recently developed, but their sensitivity is very limited because of high noise signals, originating from small source-drain current of the single Si NW. Here, we demonstrate that chemical-vapor-deposition-grown large-scale graphene/surface-modified vertical-Si-NW-arrays junctions can be utilized as diode-type biosensors for highly-sensitive and -selective detection of specific oligonucleotides. For this, a twenty-seven-base-long synthetic oligonucleotide, which is a fragment of human DENND2D promoter sequence, is first decorated as a probe on the surface of vertical Si-NW arrays, and then the complementary oligonucleotide is hybridized to the probe. This hybridization gives rise to a doping effect on the surface of Si NWs, resulting in the increase of the current in the biosensor. The current of the biosensor increases from 19 to 120% as the concentration of the target DNA varies from 0.1 to 500 nM. In contrast, such biosensing does not come into play by the use of the oligonucleotide with incompatible or mismatched sequences. Similar results are observed from photoluminescence microscopic images and spectra. The biosensors show very-uniform current changes with standard deviations ranging ~1 to ~10% by ten-times endurance tests. These results are very promising for their applications in accurate, selective, and stable biosensing. Nature Publishing Group 2016-08-18 /pmc/articles/PMC4989226/ /pubmed/27534818 http://dx.doi.org/10.1038/srep31984 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Kim, Jungkil Park, Shin-Young Kim, Sung Lee, Dae Hun Kim, Ju Hwan Kim, Jong Min Kang, Hee Han, Joong-Soo Park, Jun Woo Lee, Hosun Choi, Suk-Ho Precise and selective sensing of DNA-DNA hybridization by graphene/Si-nanowires diode-type biosensors |
title | Precise and selective sensing of DNA-DNA hybridization by graphene/Si-nanowires diode-type biosensors |
title_full | Precise and selective sensing of DNA-DNA hybridization by graphene/Si-nanowires diode-type biosensors |
title_fullStr | Precise and selective sensing of DNA-DNA hybridization by graphene/Si-nanowires diode-type biosensors |
title_full_unstemmed | Precise and selective sensing of DNA-DNA hybridization by graphene/Si-nanowires diode-type biosensors |
title_short | Precise and selective sensing of DNA-DNA hybridization by graphene/Si-nanowires diode-type biosensors |
title_sort | precise and selective sensing of dna-dna hybridization by graphene/si-nanowires diode-type biosensors |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4989226/ https://www.ncbi.nlm.nih.gov/pubmed/27534818 http://dx.doi.org/10.1038/srep31984 |
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