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A micropatterned substrate for on-surface enzymatic labelling of linearized long DNA molecules
Optical mapping of linearized DNA molecules is a promising new technology for sequence assembly and scaffolding, large structural variant detection, and diagnostics. This is currently achieved either using nanochannel confinement or by stretching single DNA molecules on a solid surface. While the fi...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6803683/ https://www.ncbi.nlm.nih.gov/pubmed/31636335 http://dx.doi.org/10.1038/s41598-019-51507-z |
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author | Varapula, Dharma LaBouff, Eric Raseley, Kaitlin Uppuluri, Lahari Ehrlich, Garth D. Noh, Moses Xiao, Ming |
author_facet | Varapula, Dharma LaBouff, Eric Raseley, Kaitlin Uppuluri, Lahari Ehrlich, Garth D. Noh, Moses Xiao, Ming |
author_sort | Varapula, Dharma |
collection | PubMed |
description | Optical mapping of linearized DNA molecules is a promising new technology for sequence assembly and scaffolding, large structural variant detection, and diagnostics. This is currently achieved either using nanochannel confinement or by stretching single DNA molecules on a solid surface. While the first method necessitates DNA labelling before linearization, the latter allows for modification post-linearization, thereby affording increased process flexibility. Each method is constrained by various physical and chemical limitations. One of the most common techniques for linearization of DNA uses a hydrophobic surface and a receding meniscus, termed molecular combing. Here, we report the development of a microfabricated surface that can not only comb the DNA molecules efficiently but also provides for sequence-specific enzymatic fluorescent DNA labelling. By modifying a glass surface with two contrasting functionalities, such that DNA binds selectively to one of the two regions, we can control DNA extension, which is known to be critical for sequence-recognition by an enzyme. Moreover, the surface modification provides enzymatic access to the DNA backbone, as well as minimizing non-specific fluorescent dye adsorption. These enhancements make the designed surface suitable for large-scale and high-resolution single DNA molecule studies. |
format | Online Article Text |
id | pubmed-6803683 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-68036832019-10-24 A micropatterned substrate for on-surface enzymatic labelling of linearized long DNA molecules Varapula, Dharma LaBouff, Eric Raseley, Kaitlin Uppuluri, Lahari Ehrlich, Garth D. Noh, Moses Xiao, Ming Sci Rep Article Optical mapping of linearized DNA molecules is a promising new technology for sequence assembly and scaffolding, large structural variant detection, and diagnostics. This is currently achieved either using nanochannel confinement or by stretching single DNA molecules on a solid surface. While the first method necessitates DNA labelling before linearization, the latter allows for modification post-linearization, thereby affording increased process flexibility. Each method is constrained by various physical and chemical limitations. One of the most common techniques for linearization of DNA uses a hydrophobic surface and a receding meniscus, termed molecular combing. Here, we report the development of a microfabricated surface that can not only comb the DNA molecules efficiently but also provides for sequence-specific enzymatic fluorescent DNA labelling. By modifying a glass surface with two contrasting functionalities, such that DNA binds selectively to one of the two regions, we can control DNA extension, which is known to be critical for sequence-recognition by an enzyme. Moreover, the surface modification provides enzymatic access to the DNA backbone, as well as minimizing non-specific fluorescent dye adsorption. These enhancements make the designed surface suitable for large-scale and high-resolution single DNA molecule studies. Nature Publishing Group UK 2019-10-21 /pmc/articles/PMC6803683/ /pubmed/31636335 http://dx.doi.org/10.1038/s41598-019-51507-z Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Varapula, Dharma LaBouff, Eric Raseley, Kaitlin Uppuluri, Lahari Ehrlich, Garth D. Noh, Moses Xiao, Ming A micropatterned substrate for on-surface enzymatic labelling of linearized long DNA molecules |
title | A micropatterned substrate for on-surface enzymatic labelling of linearized long DNA molecules |
title_full | A micropatterned substrate for on-surface enzymatic labelling of linearized long DNA molecules |
title_fullStr | A micropatterned substrate for on-surface enzymatic labelling of linearized long DNA molecules |
title_full_unstemmed | A micropatterned substrate for on-surface enzymatic labelling of linearized long DNA molecules |
title_short | A micropatterned substrate for on-surface enzymatic labelling of linearized long DNA molecules |
title_sort | micropatterned substrate for on-surface enzymatic labelling of linearized long dna molecules |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6803683/ https://www.ncbi.nlm.nih.gov/pubmed/31636335 http://dx.doi.org/10.1038/s41598-019-51507-z |
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