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Mechanical properties of nucleoprotein complexes determined by nanoindentation spectroscopy
The interplay between transcription factors, chromatin remodelers, 3-D organization, and mechanical properties of the chromatin fiber controls genome function in eukaryotes. Besides the canonical histones which fold the bulk of the chromatin into nucleosomes, histone variants create distinctive chro...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7529419/ https://www.ncbi.nlm.nih.gov/pubmed/32954931 http://dx.doi.org/10.1080/19491034.2020.1816053 |
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author | Rakshit, Tatini Melters, Daniël P. Dimitriadis, Emilios K. Dalal, Yamini |
author_facet | Rakshit, Tatini Melters, Daniël P. Dimitriadis, Emilios K. Dalal, Yamini |
author_sort | Rakshit, Tatini |
collection | PubMed |
description | The interplay between transcription factors, chromatin remodelers, 3-D organization, and mechanical properties of the chromatin fiber controls genome function in eukaryotes. Besides the canonical histones which fold the bulk of the chromatin into nucleosomes, histone variants create distinctive chromatin domains that are thought to regulate transcription, replication, DNA damage repair, and faithful chromosome segregation. Whether histone variants translate distinctive biochemical or biophysical properties to their associated chromatin structures, and whether these properties impact chromatin dynamics as the genome undergoes a multitude of transactions, is an important question in biology. Here, we describe single-molecule nanoindentation tools that we developed specifically to determine the mechanical properties of histone variant nucleosomes and their complexes. These methods join an array of cutting-edge new methods that further our quantitative understanding of the response of chromatin to intrinsic and extrinsic forces which act upon it during biological transactions in the nucleus. |
format | Online Article Text |
id | pubmed-7529419 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-75294192020-10-13 Mechanical properties of nucleoprotein complexes determined by nanoindentation spectroscopy Rakshit, Tatini Melters, Daniël P. Dimitriadis, Emilios K. Dalal, Yamini Nucleus Method The interplay between transcription factors, chromatin remodelers, 3-D organization, and mechanical properties of the chromatin fiber controls genome function in eukaryotes. Besides the canonical histones which fold the bulk of the chromatin into nucleosomes, histone variants create distinctive chromatin domains that are thought to regulate transcription, replication, DNA damage repair, and faithful chromosome segregation. Whether histone variants translate distinctive biochemical or biophysical properties to their associated chromatin structures, and whether these properties impact chromatin dynamics as the genome undergoes a multitude of transactions, is an important question in biology. Here, we describe single-molecule nanoindentation tools that we developed specifically to determine the mechanical properties of histone variant nucleosomes and their complexes. These methods join an array of cutting-edge new methods that further our quantitative understanding of the response of chromatin to intrinsic and extrinsic forces which act upon it during biological transactions in the nucleus. Taylor & Francis 2020-09-20 /pmc/articles/PMC7529419/ /pubmed/32954931 http://dx.doi.org/10.1080/19491034.2020.1816053 Text en This work was authored as part of the Contributor’s official duties as an Employee of the United States Government and is therefore a work of the United States Government. In accordance with 17 U.S.C. 105, no copyright protection is available for such works under U.S. Law. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Method Rakshit, Tatini Melters, Daniël P. Dimitriadis, Emilios K. Dalal, Yamini Mechanical properties of nucleoprotein complexes determined by nanoindentation spectroscopy |
title | Mechanical properties of nucleoprotein complexes determined by nanoindentation spectroscopy |
title_full | Mechanical properties of nucleoprotein complexes determined by nanoindentation spectroscopy |
title_fullStr | Mechanical properties of nucleoprotein complexes determined by nanoindentation spectroscopy |
title_full_unstemmed | Mechanical properties of nucleoprotein complexes determined by nanoindentation spectroscopy |
title_short | Mechanical properties of nucleoprotein complexes determined by nanoindentation spectroscopy |
title_sort | mechanical properties of nucleoprotein complexes determined by nanoindentation spectroscopy |
topic | Method |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7529419/ https://www.ncbi.nlm.nih.gov/pubmed/32954931 http://dx.doi.org/10.1080/19491034.2020.1816053 |
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