Evidence map›Paper›PMID 39217165›Full record

ArticleNature communications2024

Single-molecule force spectroscopy of toehold-mediated strand displacement.

Andreas Walbrun, Tianhe Wang, Michael Matthies, Petr Šulc, Friedrich C Simmel, Matthias Rief

Abstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
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  5. Article
  6. Article
  7. Review
  8. Review
  9. Review
  10. Article
  11. Controlling DNA-RNA strand displacement kinetics with base distribution.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  12. Review
  13. Roquin exhibits opposing effects on RNA stem-loop stability through its two ROQ domain binding sites.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  14. Review
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

6 authors.

Andreas Walbrun *Technical University of Munich, TUM School of Natural Sciences, Department of Bioscience, Center for Functional Protein Assemblies (CPA), Garching, Germany.ORCID 0009-0003-8275-1368
Tianhe Wang *Technical University of Munich, TUM School of Natural Sciences, Department of Bioscience, Garching, Germany.
Michael MatthiesTechnical University of Munich, TUM School of Natural Sciences, Department of Bioscience, Garching, Germany.ORCID 0000-0001-5979-1757
Petr ŠulcTechnical University of Munich, TUM School of Natural Sciences, Department of Bioscience, Garching, Germany.ORCID 0000-0003-1565-6769
Friedrich C SimmelTechnical University of Munich, TUM School of Natural Sciences, Department of Bioscience, Garching, Germany. simmel@tum.de.ORCID 0000-0003-3829-3446
Matthias RiefTechnical University of Munich, TUM School of Natural Sciences, Department of Bioscience, Center for Functional Protein Assemblies (CPA), Garching, Germany. matthias.rief@mytum.de.ORCID 0009-0009-7614-9470

Funding

European Union’s Horizon 2020 research and innovation program
6 · The paper itself

Abstract

Toehold-mediated strand displacement (TMSD) is extensively utilized in dynamic DNA nanotechnology and for a wide range of DNA or RNA-based reaction circuits. Investigation of TMSD kinetics typically relies on bulk fluorescence measurements providing effective, bulk-averaged reaction rates. Information on individual molecules or even base pairs is scarce. In this work, we explore the dynamics of strand displacement processes at the single-molecule level using single-molecule force spectroscopy with a microfluidics-enhanced optical trap supported by state-of-the-art coarse-grained simulations. By applying force, we can trigger and observe TMSD in real-time with microsecond and nanometer resolution. We find TMSD proceeds very rapidly under load with single step times of 1 µs. Tuning invasion efficiency by introducing mismatches allows studying thousands of forward/backward invasion events on a single molecule and analyze the kinetics of the invasion process. Extrapolation to zero force reveals single step times for DNA invading DNA four times faster than for RNA invading RNA. We also study the kinetics of DNA invading RNA, a process that in the absence of force would rarely occur. Our results reveal the importance of sequence effects for the TMSD process and have relevance for a wide range of applications in nucleic acid nanotechnology and synthetic biology.

Indexed as

DNANanotechnologyRNAKineticsMicrofluidicsMicroscopy, Atomic ForceOptical TweezersSingle Molecule ImagingSpectrum AnalysisDNARNA

Identifiers

PMID39217165
PMCPMC11365964

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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.