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Hyperstretching DNA
The three-dimensional structure of DNA is highly susceptible to changes by mechanical and biochemical cues in vivo and in vitro. In particular, large increases in base pair spacing compared to regular B-DNA are effected by mechanical (over)stretching and by intercalation of compounds that are widely...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5736724/ https://www.ncbi.nlm.nih.gov/pubmed/29259297 http://dx.doi.org/10.1038/s41467-017-02396-1 |
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author | Schakenraad, Koen Biebricher, Andreas S. Sebregts, Maarten ten Bensel, Brian Peterman, Erwin J. G. Wuite, Gijs J. L. Heller, Iddo Storm, Cornelis van der Schoot, Paul |
author_facet | Schakenraad, Koen Biebricher, Andreas S. Sebregts, Maarten ten Bensel, Brian Peterman, Erwin J. G. Wuite, Gijs J. L. Heller, Iddo Storm, Cornelis van der Schoot, Paul |
author_sort | Schakenraad, Koen |
collection | PubMed |
description | The three-dimensional structure of DNA is highly susceptible to changes by mechanical and biochemical cues in vivo and in vitro. In particular, large increases in base pair spacing compared to regular B-DNA are effected by mechanical (over)stretching and by intercalation of compounds that are widely used in biophysical/chemical assays and drug treatments. We present single-molecule experiments and a three-state statistical mechanical model that provide a quantitative understanding of the interplay between B-DNA, overstretched DNA and intercalated DNA. The predictions of this model include a hitherto unconfirmed hyperstretched state, twice the length of B-DNA. Our force-fluorescence experiments confirm this hyperstretched state and reveal its sequence dependence. These results pin down the physical principles that govern DNA mechanics under the influence of tension and biochemical reactions. A predictive understanding of the possibilities and limitations of DNA extension can guide refined exploitation of DNA in, e.g., programmable soft materials and DNA origami applications. |
format | Online Article Text |
id | pubmed-5736724 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-57367242017-12-21 Hyperstretching DNA Schakenraad, Koen Biebricher, Andreas S. Sebregts, Maarten ten Bensel, Brian Peterman, Erwin J. G. Wuite, Gijs J. L. Heller, Iddo Storm, Cornelis van der Schoot, Paul Nat Commun Article The three-dimensional structure of DNA is highly susceptible to changes by mechanical and biochemical cues in vivo and in vitro. In particular, large increases in base pair spacing compared to regular B-DNA are effected by mechanical (over)stretching and by intercalation of compounds that are widely used in biophysical/chemical assays and drug treatments. We present single-molecule experiments and a three-state statistical mechanical model that provide a quantitative understanding of the interplay between B-DNA, overstretched DNA and intercalated DNA. The predictions of this model include a hitherto unconfirmed hyperstretched state, twice the length of B-DNA. Our force-fluorescence experiments confirm this hyperstretched state and reveal its sequence dependence. These results pin down the physical principles that govern DNA mechanics under the influence of tension and biochemical reactions. A predictive understanding of the possibilities and limitations of DNA extension can guide refined exploitation of DNA in, e.g., programmable soft materials and DNA origami applications. Nature Publishing Group UK 2017-12-19 /pmc/articles/PMC5736724/ /pubmed/29259297 http://dx.doi.org/10.1038/s41467-017-02396-1 Text en © The Author(s) 2017 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 Schakenraad, Koen Biebricher, Andreas S. Sebregts, Maarten ten Bensel, Brian Peterman, Erwin J. G. Wuite, Gijs J. L. Heller, Iddo Storm, Cornelis van der Schoot, Paul Hyperstretching DNA |
title | Hyperstretching DNA |
title_full | Hyperstretching DNA |
title_fullStr | Hyperstretching DNA |
title_full_unstemmed | Hyperstretching DNA |
title_short | Hyperstretching DNA |
title_sort | hyperstretching dna |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5736724/ https://www.ncbi.nlm.nih.gov/pubmed/29259297 http://dx.doi.org/10.1038/s41467-017-02396-1 |
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