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Selectively Sized Graphene-Based Nanopores for in Situ Single Molecule Sensing
[Image: see text] The use of nanopore biosensors is set to be extremely important in developing precise single molecule detectors and providing highly sensitive advanced analysis of biological molecules. The precise tailoring of nanopore size is a significant step toward achieving this, as it would...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical Society
2015
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4543996/ https://www.ncbi.nlm.nih.gov/pubmed/26204996 http://dx.doi.org/10.1021/acsami.5b06212 |
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author | Crick, Colin R. Sze, Jasmine Y. Y. Rosillo-Lopez, Martin Salzmann, Christoph G. Edel, Joshua B. |
author_facet | Crick, Colin R. Sze, Jasmine Y. Y. Rosillo-Lopez, Martin Salzmann, Christoph G. Edel, Joshua B. |
author_sort | Crick, Colin R. |
collection | PubMed |
description | [Image: see text] The use of nanopore biosensors is set to be extremely important in developing precise single molecule detectors and providing highly sensitive advanced analysis of biological molecules. The precise tailoring of nanopore size is a significant step toward achieving this, as it would allow for a nanopore to be tuned to a corresponding analyte. The work presented here details a methodology for selectively opening nanopores in real-time. The tunable nanopores on a quartz nanopipette platform are fabricated using the electroetching of a graphene-based membrane constructed from individual graphene nanoflakes (ø ∼30 nm). The device design allows for in situ opening of the graphene membrane, from fully closed to fully opened (ø ∼25 nm), a feature that has yet to be reported in the literature. The translocation of DNA is studied as the pore size is varied, allowing for subfeatures of DNA to be detected with slower DNA translocations at smaller pore sizes, and the ability to observe trends as the pore is opened. This approach opens the door to creating a device that can be target to detect specific analytes. |
format | Online Article Text |
id | pubmed-4543996 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | American
Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-45439962015-08-24 Selectively Sized Graphene-Based Nanopores for in Situ Single Molecule Sensing Crick, Colin R. Sze, Jasmine Y. Y. Rosillo-Lopez, Martin Salzmann, Christoph G. Edel, Joshua B. ACS Appl Mater Interfaces [Image: see text] The use of nanopore biosensors is set to be extremely important in developing precise single molecule detectors and providing highly sensitive advanced analysis of biological molecules. The precise tailoring of nanopore size is a significant step toward achieving this, as it would allow for a nanopore to be tuned to a corresponding analyte. The work presented here details a methodology for selectively opening nanopores in real-time. The tunable nanopores on a quartz nanopipette platform are fabricated using the electroetching of a graphene-based membrane constructed from individual graphene nanoflakes (ø ∼30 nm). The device design allows for in situ opening of the graphene membrane, from fully closed to fully opened (ø ∼25 nm), a feature that has yet to be reported in the literature. The translocation of DNA is studied as the pore size is varied, allowing for subfeatures of DNA to be detected with slower DNA translocations at smaller pore sizes, and the ability to observe trends as the pore is opened. This approach opens the door to creating a device that can be target to detect specific analytes. American Chemical Society 2015-07-24 2015-08-19 /pmc/articles/PMC4543996/ /pubmed/26204996 http://dx.doi.org/10.1021/acsami.5b06212 Text en Copyright © 2015 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Crick, Colin R. Sze, Jasmine Y. Y. Rosillo-Lopez, Martin Salzmann, Christoph G. Edel, Joshua B. Selectively Sized Graphene-Based Nanopores for in Situ Single Molecule Sensing |
title | Selectively
Sized Graphene-Based Nanopores for in Situ Single Molecule Sensing |
title_full | Selectively
Sized Graphene-Based Nanopores for in Situ Single Molecule Sensing |
title_fullStr | Selectively
Sized Graphene-Based Nanopores for in Situ Single Molecule Sensing |
title_full_unstemmed | Selectively
Sized Graphene-Based Nanopores for in Situ Single Molecule Sensing |
title_short | Selectively
Sized Graphene-Based Nanopores for in Situ Single Molecule Sensing |
title_sort | selectively
sized graphene-based nanopores for in situ single molecule sensing |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4543996/ https://www.ncbi.nlm.nih.gov/pubmed/26204996 http://dx.doi.org/10.1021/acsami.5b06212 |
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