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A nanoscale DNA force spectrometer capable of applying tension and compression on biomolecules
Single molecule force spectroscopy is a powerful approach to probe the structure, conformational changes, and kinetic properties of biological and synthetic macromolecules. However, common approaches to apply forces to biomolecules require expensive and cumbersome equipment and relatively large prob...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8421221/ https://www.ncbi.nlm.nih.gov/pubmed/34358322 http://dx.doi.org/10.1093/nar/gkab656 |
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author | Wang, Yuchen Le, Jenny V Crocker, Kyle Darcy, Michael A Halley, Patrick D Zhao, Dengke Andrioff, Nick Croy, Cassie Poirier, Michael G Bundschuh, Ralf Castro, Carlos E |
author_facet | Wang, Yuchen Le, Jenny V Crocker, Kyle Darcy, Michael A Halley, Patrick D Zhao, Dengke Andrioff, Nick Croy, Cassie Poirier, Michael G Bundschuh, Ralf Castro, Carlos E |
author_sort | Wang, Yuchen |
collection | PubMed |
description | Single molecule force spectroscopy is a powerful approach to probe the structure, conformational changes, and kinetic properties of biological and synthetic macromolecules. However, common approaches to apply forces to biomolecules require expensive and cumbersome equipment and relatively large probes such as beads or cantilevers, which limits their use for many environments and makes integrating with other methods challenging. Furthermore, existing methods have key limitations such as an inability to apply compressive forces on single molecules. We report a nanoscale DNA force spectrometer (nDFS), which is based on a DNA origami hinge with tunable mechanical and dynamic properties. The angular free energy landscape of the nDFS can be engineered across a wide range through substitution of less than 5% of the strand components. We further incorporate a removable strut that enables reversible toggling of the nDFS between open and closed states to allow for actuated application of tensile and compressive forces. We demonstrate the ability to apply compressive forces by inducing a large bend in a 249bp DNA molecule, and tensile forces by inducing DNA unwrapping of a nucleosome sample. These results establish a versatile tool for force spectroscopy and robust methods for designing nanoscale mechanical devices with tunable force application. |
format | Online Article Text |
id | pubmed-8421221 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-84212212021-09-09 A nanoscale DNA force spectrometer capable of applying tension and compression on biomolecules Wang, Yuchen Le, Jenny V Crocker, Kyle Darcy, Michael A Halley, Patrick D Zhao, Dengke Andrioff, Nick Croy, Cassie Poirier, Michael G Bundschuh, Ralf Castro, Carlos E Nucleic Acids Res Synthetic Biology and Bioengineering Single molecule force spectroscopy is a powerful approach to probe the structure, conformational changes, and kinetic properties of biological and synthetic macromolecules. However, common approaches to apply forces to biomolecules require expensive and cumbersome equipment and relatively large probes such as beads or cantilevers, which limits their use for many environments and makes integrating with other methods challenging. Furthermore, existing methods have key limitations such as an inability to apply compressive forces on single molecules. We report a nanoscale DNA force spectrometer (nDFS), which is based on a DNA origami hinge with tunable mechanical and dynamic properties. The angular free energy landscape of the nDFS can be engineered across a wide range through substitution of less than 5% of the strand components. We further incorporate a removable strut that enables reversible toggling of the nDFS between open and closed states to allow for actuated application of tensile and compressive forces. We demonstrate the ability to apply compressive forces by inducing a large bend in a 249bp DNA molecule, and tensile forces by inducing DNA unwrapping of a nucleosome sample. These results establish a versatile tool for force spectroscopy and robust methods for designing nanoscale mechanical devices with tunable force application. Oxford University Press 2021-08-06 /pmc/articles/PMC8421221/ /pubmed/34358322 http://dx.doi.org/10.1093/nar/gkab656 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of Nucleic Acids Research. 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 reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Synthetic Biology and Bioengineering Wang, Yuchen Le, Jenny V Crocker, Kyle Darcy, Michael A Halley, Patrick D Zhao, Dengke Andrioff, Nick Croy, Cassie Poirier, Michael G Bundschuh, Ralf Castro, Carlos E A nanoscale DNA force spectrometer capable of applying tension and compression on biomolecules |
title | A nanoscale DNA force spectrometer capable of applying tension and compression on biomolecules |
title_full | A nanoscale DNA force spectrometer capable of applying tension and compression on biomolecules |
title_fullStr | A nanoscale DNA force spectrometer capable of applying tension and compression on biomolecules |
title_full_unstemmed | A nanoscale DNA force spectrometer capable of applying tension and compression on biomolecules |
title_short | A nanoscale DNA force spectrometer capable of applying tension and compression on biomolecules |
title_sort | nanoscale dna force spectrometer capable of applying tension and compression on biomolecules |
topic | Synthetic Biology and Bioengineering |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8421221/ https://www.ncbi.nlm.nih.gov/pubmed/34358322 http://dx.doi.org/10.1093/nar/gkab656 |
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