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Multicolor and Erasable DNA Photolithography
[Image: see text] The immobilization of DNA molecules onto a solid support is a crucial step in biochip research and related applications. In this work, we report a DNA photolithography method based on photocleavage of 2-nitrobenzyl linker-modified DNA strands. These strands were subjected to ultrav...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4372106/ https://www.ncbi.nlm.nih.gov/pubmed/24988147 http://dx.doi.org/10.1021/nn5024472 |
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author | Huang, Fujian Xu, Huaguo Tan, Weihong Liang, Haojun |
author_facet | Huang, Fujian Xu, Huaguo Tan, Weihong Liang, Haojun |
author_sort | Huang, Fujian |
collection | PubMed |
description | [Image: see text] The immobilization of DNA molecules onto a solid support is a crucial step in biochip research and related applications. In this work, we report a DNA photolithography method based on photocleavage of 2-nitrobenzyl linker-modified DNA strands. These strands were subjected to ultraviolet light irradiation to generate multiple short DNA strands in a programmable manner. Coupling the toehold-mediated DNA strand-displacement reaction with DNA photolithography enabled the fabrication of a DNA chip surface with multifunctional DNA patterns having complex geometrical structures at the microscale level. The erasable DNA photolithography strategy was developed to allow different paintings on the same chip. Furthermore, the asymmetrical modification of colloidal particles was carried out by using this photolithography strategy. This strategy has broad applications in biosensors, nanodevices, and DNA-nanostructure fabrication. |
format | Online Article Text |
id | pubmed-4372106 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-43721062015-07-02 Multicolor and Erasable DNA Photolithography Huang, Fujian Xu, Huaguo Tan, Weihong Liang, Haojun ACS Nano [Image: see text] The immobilization of DNA molecules onto a solid support is a crucial step in biochip research and related applications. In this work, we report a DNA photolithography method based on photocleavage of 2-nitrobenzyl linker-modified DNA strands. These strands were subjected to ultraviolet light irradiation to generate multiple short DNA strands in a programmable manner. Coupling the toehold-mediated DNA strand-displacement reaction with DNA photolithography enabled the fabrication of a DNA chip surface with multifunctional DNA patterns having complex geometrical structures at the microscale level. The erasable DNA photolithography strategy was developed to allow different paintings on the same chip. Furthermore, the asymmetrical modification of colloidal particles was carried out by using this photolithography strategy. This strategy has broad applications in biosensors, nanodevices, and DNA-nanostructure fabrication. American Chemical Society 2014-07-02 2014-07-22 /pmc/articles/PMC4372106/ /pubmed/24988147 http://dx.doi.org/10.1021/nn5024472 Text en Copyright © 2014 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 | Huang, Fujian Xu, Huaguo Tan, Weihong Liang, Haojun Multicolor and Erasable DNA Photolithography |
title | Multicolor and Erasable DNA Photolithography |
title_full | Multicolor and Erasable DNA Photolithography |
title_fullStr | Multicolor and Erasable DNA Photolithography |
title_full_unstemmed | Multicolor and Erasable DNA Photolithography |
title_short | Multicolor and Erasable DNA Photolithography |
title_sort | multicolor and erasable dna photolithography |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4372106/ https://www.ncbi.nlm.nih.gov/pubmed/24988147 http://dx.doi.org/10.1021/nn5024472 |
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