Evidence map›Paper›PMID 24019238›Full record

ArticleNucleic acids research2013

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

Niranjan Srinivas, Thomas E Ouldridge, Petr Sulc, Joseph M Schaeffer, Bernard Yurke, Ard A Louis, Jonathan P K Doye, Erik Winfree

Abstract read
In one paragraph

Article in Nucleic acids research, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 171 papers.

0numbers the graph read from it
0cells of the map it votes in
171citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

171 citing papers in PubMed.

  1. Article
  2. Review
  3. Enzymatic DNA Reaction Networks for Orchestrating Stimuli-Dependent Temporal Molecular Pulse.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  4. Article
  5. How do RNA molecules distinguish self from non-self?Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  6. Article
  7. Programming DNA machines to move.Nature reviews. Chemistry · 2026
    Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Controlling DNA-RNA strand displacement kinetics with base distribution.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  18. Review
  19. How We Simulate DNA Origami.Small methods · 2025
    Article
  20. Review

111 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Niranjan SrinivasComputation and Neural Systems, California Institute of Technology, Pasadena, CA 91125, USA, Rudolph Peierls Centre for Theoretical Physics, Department of Physics, University of Oxford, Oxford OX1 3NP, UK, Computer Science, California Institute of Technology, Pasadena, CA 91125, USA, Departments of Electrical and Computer Engineering, Materials Science and Engineering, Boise State University, ID83725, USA, Physical and Theoretical Chemistry Laboratory, Department of Chemistry, University of Oxford, Oxford OX1 3QZ, UK and Bioengineering, California Institute of Technology, Pasadena, CA 91125, USA.
Thomas E Ouldridge
Petr Sulc
Joseph M Schaeffer
Bernard Yurke
Ard A Louis
Jonathan P K Doye
Erik Winfree

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Indexed as

AlgorithmsBiophysical PhenomenaDNAKineticsModels, MolecularThermodynamicsDNA

Identifiers

PMID24019238
PMCPMC3905871

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.