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On the biophysics and kinetics of toehold-mediated DNA strand displacement

Dynamic DNA nanotechnology often uses toehold-mediated strand displacement for controlling reaction kinetics. Although the dependence of strand displacement kinetics on toehold length has been experimentally characterized and phenomenologically modeled, detailed biophysical understanding has remaine...

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Autores principales: Srinivas, Niranjan, Ouldridge, Thomas E., Šulc, Petr, Schaeffer, Joseph M., Yurke, Bernard, Louis, Ard A., Doye, Jonathan P. K., Winfree, Erik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3905871/
https://www.ncbi.nlm.nih.gov/pubmed/24019238
http://dx.doi.org/10.1093/nar/gkt801
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author Srinivas, Niranjan
Ouldridge, Thomas E.
Šulc, Petr
Schaeffer, Joseph M.
Yurke, Bernard
Louis, Ard A.
Doye, Jonathan P. K.
Winfree, Erik
author_facet Srinivas, Niranjan
Ouldridge, Thomas E.
Šulc, Petr
Schaeffer, Joseph M.
Yurke, Bernard
Louis, Ard A.
Doye, Jonathan P. K.
Winfree, Erik
author_sort Srinivas, Niranjan
collection PubMed
description Dynamic DNA nanotechnology often uses toehold-mediated strand displacement for controlling reaction kinetics. Although the dependence of strand displacement kinetics on toehold length has been experimentally characterized and phenomenologically modeled, detailed biophysical understanding has remained elusive. Here, we study strand displacement at multiple levels of detail, using an intuitive model of a random walk on a 1D energy landscape, a secondary structure kinetics model with single base-pair steps and a coarse-grained molecular model that incorporates 3D geometric and steric effects. Further, we experimentally investigate the thermodynamics of three-way branch migration. Two factors explain the dependence of strand displacement kinetics on toehold length: (i) the physical process by which a single step of branch migration occurs is significantly slower than the fraying of a single base pair and (ii) initiating branch migration incurs a thermodynamic penalty, not captured by state-of-the-art nearest neighbor models of DNA, due to the additional overhang it engenders at the junction. Our findings are consistent with previously measured or inferred rates for hybridization, fraying and branch migration, and they provide a biophysical explanation of strand displacement kinetics. Our work paves the way for accurate modeling of strand displacement cascades, which would facilitate the simulation and construction of more complex molecular systems.
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spelling pubmed-39058712014-01-29 On the biophysics and kinetics of toehold-mediated DNA strand displacement Srinivas, Niranjan Ouldridge, Thomas E. Šulc, Petr Schaeffer, Joseph M. Yurke, Bernard Louis, Ard A. Doye, Jonathan P. K. Winfree, Erik Nucleic Acids Res Synthetic Biology and Chemistry Dynamic DNA nanotechnology often uses toehold-mediated strand displacement for controlling reaction kinetics. Although the dependence of strand displacement kinetics on toehold length has been experimentally characterized and phenomenologically modeled, detailed biophysical understanding has remained elusive. Here, we study strand displacement at multiple levels of detail, using an intuitive model of a random walk on a 1D energy landscape, a secondary structure kinetics model with single base-pair steps and a coarse-grained molecular model that incorporates 3D geometric and steric effects. Further, we experimentally investigate the thermodynamics of three-way branch migration. Two factors explain the dependence of strand displacement kinetics on toehold length: (i) the physical process by which a single step of branch migration occurs is significantly slower than the fraying of a single base pair and (ii) initiating branch migration incurs a thermodynamic penalty, not captured by state-of-the-art nearest neighbor models of DNA, due to the additional overhang it engenders at the junction. Our findings are consistent with previously measured or inferred rates for hybridization, fraying and branch migration, and they provide a biophysical explanation of strand displacement kinetics. Our work paves the way for accurate modeling of strand displacement cascades, which would facilitate the simulation and construction of more complex molecular systems. Oxford University Press 2013-12 2013-09-07 /pmc/articles/PMC3905871/ /pubmed/24019238 http://dx.doi.org/10.1093/nar/gkt801 Text en © The Author(s) 2013. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Synthetic Biology and Chemistry
Srinivas, Niranjan
Ouldridge, Thomas E.
Šulc, Petr
Schaeffer, Joseph M.
Yurke, Bernard
Louis, Ard A.
Doye, Jonathan P. K.
Winfree, Erik
On the biophysics and kinetics of toehold-mediated DNA strand displacement
title On the biophysics and kinetics of toehold-mediated DNA strand displacement
title_full On the biophysics and kinetics of toehold-mediated DNA strand displacement
title_fullStr On the biophysics and kinetics of toehold-mediated DNA strand displacement
title_full_unstemmed On the biophysics and kinetics of toehold-mediated DNA strand displacement
title_short On the biophysics and kinetics of toehold-mediated DNA strand displacement
title_sort on the biophysics and kinetics of toehold-mediated dna strand displacement
topic Synthetic Biology and Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3905871/
https://www.ncbi.nlm.nih.gov/pubmed/24019238
http://dx.doi.org/10.1093/nar/gkt801
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