Evidence map›Paper›PMID 39344156›Full record

ArticleACS nano2024

DNA-Based Molecular Clamp for Probing Protein Interactions and Structure under Force.

Minhwan Chung, Kun Zhou, John T Powell, Chenxiang Lin, Martin A Schwartz

Abstract read
In one paragraph

Article in ACS nano, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Mechanomedicine: Present state and future promise.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  2. Article
  3. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Minhwan ChungYale Cardiovascular Research Center, Department of Internal Medicine (Cardiology), Yale University School of Medicine, New Haven, Connecticut 06511, United States.ORCID 0000-0001-6720-7514
John T Powell
Martin A SchwartzYale Cardiovascular Research Center, Department of Internal Medicine (Cardiology), Yale University School of Medicine, New Haven, Connecticut 06511, United States.

Funding

Metabolism and cell cycle as mediators of fluid shear stress effects on vascular endothelium in health and diseaseR01HL175052 · NHLBI · YALE UNIVERSITY · PI Martin A Schwartz · 2024 to 2026
$2.4M
Fluid shear stress mechanotransduction at endothelial cell-cell junctionsR01HL155543 · NHLBI · YALE UNIVERSITY · PI LIN, CHENXIANG, SCHWARTZ, MARTIN A · 2021 to 2024
$2.3M
NHLBI NIH HHS R01 HL155543NHLBI NIH HHS R01 HL175052
6 · The paper itself

Abstract

Cellular mechanotransduction, a process central to cell biology, embryogenesis, adult physiology, and multiple diseases, is thought to be mediated by force-driven changes in protein conformation that control protein function. However, methods to study proteins under defined mechanical loads on a biochemical scale are lacking. We report the development of a DNA-based device in which the transition between single- and double-stranded DNA applies tension to an attached protein. Using a fragment of the talin rod domain as a test case, negative-stain electron microscopy reveals programmable extension, while pull down assays show tension-induced binding to two ligands, ARPC5L and vinculin, known to bind to cryptic sites inside the talin structure. These results demonstrate the utility of the DNA clamp for biochemical studies and potential structural analysis.

Indexed as

DNATalinMechanotransduction, CellularProtein BindingProtein ConformationVinculinDNATalinVinculinDNA nanotechnologyintegrinmechanotransductiontalin1tension

Identifiers

PMID39344156
PMCPMC11518680

What Socratic holds

Textmetadata
LicenceTDM
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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 Socratic graph.