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Detection of Sub-fM DNA with Target Recycling and Self-Assembly Amplification on Graphene Field-Effect Biosensors
[Image: see text] All-electronic DNA biosensors based on graphene field-effect transistors (GFETs) offer the prospect of simple and cost-effective diagnostics. For GFET sensors based on complementary probe DNA, the sensitivity is limited by the binding affinity of the target oligonucleotide, in the...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6002779/ https://www.ncbi.nlm.nih.gov/pubmed/29768011 http://dx.doi.org/10.1021/acs.nanolett.8b00572 |
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author | Gao, Zhaoli Xia, Han Zauberman, Jonathan Tomaiuolo, Maurizio Ping, Jinglei Zhang, Qicheng Ducos, Pedro Ye, Huacheng Wang, Sheng Yang, Xinping Lubna, Fahmida Luo, Zhengtang Ren, Li Johnson, Alan T. Charlie |
author_facet | Gao, Zhaoli Xia, Han Zauberman, Jonathan Tomaiuolo, Maurizio Ping, Jinglei Zhang, Qicheng Ducos, Pedro Ye, Huacheng Wang, Sheng Yang, Xinping Lubna, Fahmida Luo, Zhengtang Ren, Li Johnson, Alan T. Charlie |
author_sort | Gao, Zhaoli |
collection | PubMed |
description | [Image: see text] All-electronic DNA biosensors based on graphene field-effect transistors (GFETs) offer the prospect of simple and cost-effective diagnostics. For GFET sensors based on complementary probe DNA, the sensitivity is limited by the binding affinity of the target oligonucleotide, in the nM range for 20 mer targets. We report a ∼20 000× improvement in sensitivity through the use of engineered hairpin probe DNA that allows for target recycling and hybridization chain reaction. This enables detection of 21 mer target DNA at sub-fM concentration and provides superior specificity against single-base mismatched oligomers. The work is based on a scalable fabrication process for biosensor arrays that is suitable for multiplexed detection. This approach overcomes the binding-affinity-dependent sensitivity of nucleic acid biosensors and offers a pathway toward multiplexed and label-free nucleic acid testing with high accuracy and selectivity. |
format | Online Article Text |
id | pubmed-6002779 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-60027792018-06-19 Detection of Sub-fM DNA with Target Recycling and Self-Assembly Amplification on Graphene Field-Effect Biosensors Gao, Zhaoli Xia, Han Zauberman, Jonathan Tomaiuolo, Maurizio Ping, Jinglei Zhang, Qicheng Ducos, Pedro Ye, Huacheng Wang, Sheng Yang, Xinping Lubna, Fahmida Luo, Zhengtang Ren, Li Johnson, Alan T. Charlie Nano Lett [Image: see text] All-electronic DNA biosensors based on graphene field-effect transistors (GFETs) offer the prospect of simple and cost-effective diagnostics. For GFET sensors based on complementary probe DNA, the sensitivity is limited by the binding affinity of the target oligonucleotide, in the nM range for 20 mer targets. We report a ∼20 000× improvement in sensitivity through the use of engineered hairpin probe DNA that allows for target recycling and hybridization chain reaction. This enables detection of 21 mer target DNA at sub-fM concentration and provides superior specificity against single-base mismatched oligomers. The work is based on a scalable fabrication process for biosensor arrays that is suitable for multiplexed detection. This approach overcomes the binding-affinity-dependent sensitivity of nucleic acid biosensors and offers a pathway toward multiplexed and label-free nucleic acid testing with high accuracy and selectivity. American Chemical Society 2018-05-16 2018-06-13 /pmc/articles/PMC6002779/ /pubmed/29768011 http://dx.doi.org/10.1021/acs.nanolett.8b00572 Text en Copyright © 2018 American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited. |
spellingShingle | Gao, Zhaoli Xia, Han Zauberman, Jonathan Tomaiuolo, Maurizio Ping, Jinglei Zhang, Qicheng Ducos, Pedro Ye, Huacheng Wang, Sheng Yang, Xinping Lubna, Fahmida Luo, Zhengtang Ren, Li Johnson, Alan T. Charlie Detection of Sub-fM DNA with Target Recycling and Self-Assembly Amplification on Graphene Field-Effect Biosensors |
title | Detection of Sub-fM DNA with Target Recycling and
Self-Assembly Amplification on Graphene Field-Effect Biosensors |
title_full | Detection of Sub-fM DNA with Target Recycling and
Self-Assembly Amplification on Graphene Field-Effect Biosensors |
title_fullStr | Detection of Sub-fM DNA with Target Recycling and
Self-Assembly Amplification on Graphene Field-Effect Biosensors |
title_full_unstemmed | Detection of Sub-fM DNA with Target Recycling and
Self-Assembly Amplification on Graphene Field-Effect Biosensors |
title_short | Detection of Sub-fM DNA with Target Recycling and
Self-Assembly Amplification on Graphene Field-Effect Biosensors |
title_sort | detection of sub-fm dna with target recycling and
self-assembly amplification on graphene field-effect biosensors |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6002779/ https://www.ncbi.nlm.nih.gov/pubmed/29768011 http://dx.doi.org/10.1021/acs.nanolett.8b00572 |
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