Evidence map›Paper›PMID 38374280›Full record

ArticleScientific reports2024

Cooperative control of a DNA origami force sensor.

Ariel Robbins, Hazen Hildebolt, Michael Neuhoff, Peter Beshay, Jessica O Winter, Carlos E Castro, Ralf Bundschuh, Michael G Poirier

Abstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Article
  3. The effect of long-term ambient storage on the morphology of adhered DNA origami.Computational and structural biotechnology journal · 2026
    Article
  4. Unraveling the Folding Dynamics of DNA Origami Structures.Small (Weinheim an der Bergstrasse, Germany) · 2025
    Article
  5. Article
  6. Article
  7. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Ariel RobbinsBiophysics Graduate Program, The Ohio State University, Columbus, OH, 43210, USA.
Hazen HildeboltDepartment of Physics, The Ohio State University, Columbus, OH, 43210, USA.
Michael NeuhoffDepartment of Physics, The Ohio State University, Columbus, OH, 43210, USA.
Peter BeshayDepartment of Mechanical and Aerospace Engineering, The Ohio State University, Columbus, OH, 43210, USA.
Jessica O WinterBiophysics Graduate Program, The Ohio State University, Columbus, OH, 43210, USA.
Carlos E CastroBiophysics Graduate Program, The Ohio State University, Columbus, OH, 43210, USA.
Ralf BundschuhBiophysics Graduate Program, The Ohio State University, Columbus, OH, 43210, USA.
Michael G PoirierBiophysics Graduate Program, The Ohio State University, Columbus, OH, 43210, USA. poirier.18@osu.edu.

Funding

Translational Therapeutics Research Program (TT)P30CA016058 · NCI · OHIO STATE UNIVERSITY · PI Tasleem J Padamsee · 1985 to 2026
$132.3M
Mechanisms of chromatin regulation of transcriptionR35GM139564 · NIGMS · OHIO STATE UNIVERSITY · PI POIRIER, MICHAEL GUY · 2021 to 2025
$3.6M
NCI NIH HHS P30 CA016058NIGMS NIH HHS R35 GM139564
6 · The paper itself

Abstract

Biomolecular systems are dependent on a complex interplay of forces. Modern force spectroscopy techniques provide means of interrogating these forces, but they are not optimized for studies in constrained environments as they require attachment to micron-scale probes such as beads or cantilevers. Nanomechanical devices are a promising alternative, but this requires versatile designs that can be tuned to respond to a wide range of forces. We investigate the properties of a nanoscale force sensitive DNA origami device which is highly customizable in geometry, functionalization, and mechanical properties. The device, referred to as the NanoDyn, has a binary (open or closed) response to an applied force by undergoing a reversible structural transition. The transition force is tuned with minor alterations of 1 to 3 DNA oligonucleotides and spans tens of picoNewtons (pN). The DNA oligonucleotide design parameters also strongly influence the efficiency of resetting the initial state, with higher stability devices (≳10 pN) resetting more reliably during repeated force-loading cycles. Finally, we show the opening force is tunable in real time by adding a single DNA oligonucleotide. These results establish the potential of the NanoDyn as a versatile force sensor and provide fundamental insights into how design parameters modulate mechanical and dynamic properties.

Indexed as

NanostructuresDNAMechanical PhenomenaMicroscopy, Atomic ForceNucleic Acid ConformationOligonucleotidesDNAOligonucleotides

Identifiers

PMID38374280
PMCPMC10876929

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Registered trials

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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.