Evidence map›Paper›PMID 34059812›Full record

ArticleNature cell biology2021

A reversible shearing DNA probe for visualizing mechanically strong receptors in living cells.

Hongyun Li, Chen Zhang, Yuru Hu, Pengxiang Liu, Feng Sun, Wei Chen, Xinghua Zhang, Jie Ma, Wenxu Wang, Liang Wang and 2 more

Abstract readVideo-Audio Media
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In one paragraph

Article in Nature cell biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
8.6field-weighted citation impact, top 2% of its field
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

39 citing papers in PubMed, 86 citations in OpenAlex.

  1. Review
  2. Traction Force Microscopy with DNA FluoroCubes.Langmuir : the ACS journal of surfaces and colloids · 2026
    Article
  3. Review
  4. Force-dependent structural dynamics of the giant nesprin-2.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  5. Review
  6. Capped high-force integrin bond lifetimes and spacing-tuned binding frequency drive rapid fibroblast migration.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
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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

12 authors at 2 institutions in 1 country.

Hongyun LiThe Institute for Advanced Studies, Wuhan University, Wuhan, China.
Chen ZhangCollege of Life Sciences, State Key Laboratory of Virology, Wuhan University, Wuhan, China.
Yuru HuThe Institute for Advanced Studies, Wuhan University, Wuhan, China.
Pengxiang LiuThe Institute for Advanced Studies, Wuhan University, Wuhan, China.
Feng SunThe Institute for Advanced Studies, Wuhan University, Wuhan, China.
Wei ChenThe Institute for Advanced Studies, Wuhan University, Wuhan, China.
Xinghua ZhangThe Institute for Advanced Studies, Wuhan University, Wuhan, China.ORCID http://orcid.org/0000-0002-9487-191X
Jie MaSchool of Physics, Sun Yat-sen University, Guangzhou, China.
Wenxu WangThe Institute for Advanced Studies, Wuhan University, Wuhan, China.
Liang WangThe Institute for Advanced Studies, Wuhan University, Wuhan, China.
Piyu WuThe Institute for Advanced Studies, Wuhan University, Wuhan, China.
Zheng LiuThe Institute for Advanced Studies, Wuhan University, Wuhan, China. zheng.liu@whu.edu.cn.ORCID http://orcid.org/0000-0002-4252-4617
Wuhan University · CNSun Yat-sen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In the last decade, DNA-based tension sensors have made significant contributions to the study of the importance of mechanical forces in many biological systems. Albeit successful, one shortcoming of these techniques is their inability to reversibly measure receptor forces in a higher regime (that is, >20 pN), which limits our understanding of the molecular details of mechanochemical transduction in living cells. Here, we developed a reversible shearing DNA-based tension probe (RSDTP) for probing molecular piconewton-scale forces between 4 and 60 pN transmitted by cells. Using these probes, we can easily distinguish the differences in force-bearing integrins without perturbing adhesion biology and reveal that a strong force-bearing integrin cluster can serve as a 'mechanical pivot' to maintain focal adhesion architecture and facilitate its maturation. The benefits of the RSDTP include a high dynamic range, reversibility and single-molecule sensitivity, all of which will facilitate a better understanding of the molecular mechanisms of mechanobiology.

Indexed as

Mechanotransduction, CellularMicroscopy, FluorescenceMicroscopy, VideoAnimalsBiosensing TechniquesCell AdhesionCell MovementDNA ProbesFluorescent DyesFocal AdhesionsIntegrinsMiceNanotechnologyNIH 3T3 CellsNucleic Acid ConformationStress, MechanicalDNA ProbesFluorescent DyesIntegrins

Identifiers

PMID34059812
OpenAlexW3164720541

What OpenQuestion holds

Textmetadata
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.