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Single-Molecule Reaction Chemistry in Patterned Nanowells
[Image: see text] A new approach to synthetic chemistry is performed in ultraminiaturized, nanofabricated reaction chambers. Using lithographically defined nanowells, we achieve single-point covalent chemistry on hundreds of individual carbon nanotube transistors, providing robust statistics and unp...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5176326/ https://www.ncbi.nlm.nih.gov/pubmed/27270004 http://dx.doi.org/10.1021/acs.nanolett.6b02149 |
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author | Bouilly, Delphine Hon, Jason Daly, Nathan S. Trocchia, Scott Vernick, Sefi Yu, Jaeeun Warren, Steven Wu, Ying Gonzalez, Ruben L. Shepard, Kenneth L. Nuckolls, Colin |
author_facet | Bouilly, Delphine Hon, Jason Daly, Nathan S. Trocchia, Scott Vernick, Sefi Yu, Jaeeun Warren, Steven Wu, Ying Gonzalez, Ruben L. Shepard, Kenneth L. Nuckolls, Colin |
author_sort | Bouilly, Delphine |
collection | PubMed |
description | [Image: see text] A new approach to synthetic chemistry is performed in ultraminiaturized, nanofabricated reaction chambers. Using lithographically defined nanowells, we achieve single-point covalent chemistry on hundreds of individual carbon nanotube transistors, providing robust statistics and unprecedented spatial resolution in adduct position. Each device acts as a sensor to detect, in real-time and through quantized changes in conductance, single-point functionalization of the nanotube as well as consecutive chemical reactions, molecular interactions, and molecular conformational changes occurring on the resulting single-molecule probe. In particular, we use a set of sequential bioconjugation reactions to tether a single-strand of DNA to the device and record its repeated, reversible folding into a G-quadruplex structure. The stable covalent tether allows us to measure the same molecule in different solutions, revealing the characteristic increased stability of the G-quadruplex structure in the presence of potassium ions (K(+)) versus sodium ions (Na(+)). Nanowell-confined reaction chemistry on carbon nanotube devices offers a versatile method to isolate and monitor individual molecules during successive chemical reactions over an extended period of time. |
format | Online Article Text |
id | pubmed-5176326 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-51763262016-12-22 Single-Molecule Reaction Chemistry in Patterned Nanowells Bouilly, Delphine Hon, Jason Daly, Nathan S. Trocchia, Scott Vernick, Sefi Yu, Jaeeun Warren, Steven Wu, Ying Gonzalez, Ruben L. Shepard, Kenneth L. Nuckolls, Colin Nano Lett [Image: see text] A new approach to synthetic chemistry is performed in ultraminiaturized, nanofabricated reaction chambers. Using lithographically defined nanowells, we achieve single-point covalent chemistry on hundreds of individual carbon nanotube transistors, providing robust statistics and unprecedented spatial resolution in adduct position. Each device acts as a sensor to detect, in real-time and through quantized changes in conductance, single-point functionalization of the nanotube as well as consecutive chemical reactions, molecular interactions, and molecular conformational changes occurring on the resulting single-molecule probe. In particular, we use a set of sequential bioconjugation reactions to tether a single-strand of DNA to the device and record its repeated, reversible folding into a G-quadruplex structure. The stable covalent tether allows us to measure the same molecule in different solutions, revealing the characteristic increased stability of the G-quadruplex structure in the presence of potassium ions (K(+)) versus sodium ions (Na(+)). Nanowell-confined reaction chemistry on carbon nanotube devices offers a versatile method to isolate and monitor individual molecules during successive chemical reactions over an extended period of time. American Chemical Society 2016-06-07 2016-07-13 /pmc/articles/PMC5176326/ /pubmed/27270004 http://dx.doi.org/10.1021/acs.nanolett.6b02149 Text en Copyright © 2016 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 | Bouilly, Delphine Hon, Jason Daly, Nathan S. Trocchia, Scott Vernick, Sefi Yu, Jaeeun Warren, Steven Wu, Ying Gonzalez, Ruben L. Shepard, Kenneth L. Nuckolls, Colin Single-Molecule Reaction Chemistry in Patterned Nanowells |
title | Single-Molecule Reaction Chemistry in Patterned Nanowells |
title_full | Single-Molecule Reaction Chemistry in Patterned Nanowells |
title_fullStr | Single-Molecule Reaction Chemistry in Patterned Nanowells |
title_full_unstemmed | Single-Molecule Reaction Chemistry in Patterned Nanowells |
title_short | Single-Molecule Reaction Chemistry in Patterned Nanowells |
title_sort | single-molecule reaction chemistry in patterned nanowells |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5176326/ https://www.ncbi.nlm.nih.gov/pubmed/27270004 http://dx.doi.org/10.1021/acs.nanolett.6b02149 |
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