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Effect of Temperature on the Intrinsic Flexibility of DNA and Its Interaction with Architectural Proteins
[Image: see text] The helical structure of double-stranded DNA is destabilized by increasing temperature. Above a critical temperature (the melting temperature), the two strands in duplex DNA become fully separated. Below this temperature, the structural effects are localized. Using tethered particl...
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/PMC5451147/ https://www.ncbi.nlm.nih.gov/pubmed/25291500 http://dx.doi.org/10.1021/bi500344j |
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author | Driessen, Rosalie P. C. Sitters, Gerrit Laurens, Niels Moolenaar, Geri F. Wuite, Gijs J. L. Goosen, Nora Dame, Remus Th. |
author_facet | Driessen, Rosalie P. C. Sitters, Gerrit Laurens, Niels Moolenaar, Geri F. Wuite, Gijs J. L. Goosen, Nora Dame, Remus Th. |
author_sort | Driessen, Rosalie P. C. |
collection | PubMed |
description | [Image: see text] The helical structure of double-stranded DNA is destabilized by increasing temperature. Above a critical temperature (the melting temperature), the two strands in duplex DNA become fully separated. Below this temperature, the structural effects are localized. Using tethered particle motion in a temperature-controlled sample chamber, we systematically investigated the effect of increasing temperature on DNA structure and the interplay between this effect and protein binding. Our measurements revealed that (1) increasing temperature enhances DNA flexibility, effectively leading to more compact folding of the double-stranded DNA chain, and (2) temperature differentially affects different types of DNA-bending chromatin proteins from mesophilic and thermophilic organisms. Thus, our findings aid in understanding genome organization in organisms thriving at moderate as well as extreme temperatures. Moreover, our results underscore the importance of carefully controlling and measuring temperature in single-molecule DNA (micromanipulation) experiments. |
format | Online Article Text |
id | pubmed-5451147 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | American
Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-54511472017-06-01 Effect of Temperature on the Intrinsic Flexibility of DNA and Its Interaction with Architectural Proteins Driessen, Rosalie P. C. Sitters, Gerrit Laurens, Niels Moolenaar, Geri F. Wuite, Gijs J. L. Goosen, Nora Dame, Remus Th. Biochemistry [Image: see text] The helical structure of double-stranded DNA is destabilized by increasing temperature. Above a critical temperature (the melting temperature), the two strands in duplex DNA become fully separated. Below this temperature, the structural effects are localized. Using tethered particle motion in a temperature-controlled sample chamber, we systematically investigated the effect of increasing temperature on DNA structure and the interplay between this effect and protein binding. Our measurements revealed that (1) increasing temperature enhances DNA flexibility, effectively leading to more compact folding of the double-stranded DNA chain, and (2) temperature differentially affects different types of DNA-bending chromatin proteins from mesophilic and thermophilic organisms. Thus, our findings aid in understanding genome organization in organisms thriving at moderate as well as extreme temperatures. Moreover, our results underscore the importance of carefully controlling and measuring temperature in single-molecule DNA (micromanipulation) experiments. American Chemical Society 2014-10-07 2014-10-21 /pmc/articles/PMC5451147/ /pubmed/25291500 http://dx.doi.org/10.1021/bi500344j Text en Copyright © 2014 American Chemical Society This is an open access article published under a Creative Commons Non-Commercial No Derivative Works (CC-BY-NC-ND) Attribution License (http://pubs.acs.org/page/policy/authorchoice_ccbyncnd_termsofuse.html) , which permits copying and redistribution of the article, and creation of adaptations, all for non-commercial purposes. |
spellingShingle | Driessen, Rosalie P. C. Sitters, Gerrit Laurens, Niels Moolenaar, Geri F. Wuite, Gijs J. L. Goosen, Nora Dame, Remus Th. Effect of Temperature on the Intrinsic Flexibility of DNA and Its Interaction with Architectural Proteins |
title | Effect of Temperature
on the Intrinsic Flexibility
of DNA and Its Interaction with Architectural Proteins |
title_full | Effect of Temperature
on the Intrinsic Flexibility
of DNA and Its Interaction with Architectural Proteins |
title_fullStr | Effect of Temperature
on the Intrinsic Flexibility
of DNA and Its Interaction with Architectural Proteins |
title_full_unstemmed | Effect of Temperature
on the Intrinsic Flexibility
of DNA and Its Interaction with Architectural Proteins |
title_short | Effect of Temperature
on the Intrinsic Flexibility
of DNA and Its Interaction with Architectural Proteins |
title_sort | effect of temperature
on the intrinsic flexibility
of dna and its interaction with architectural proteins |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5451147/ https://www.ncbi.nlm.nih.gov/pubmed/25291500 http://dx.doi.org/10.1021/bi500344j |
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