Evidence map›Paper›PMID 35902570›Full record

ArticleNature communications2022

A modular spring-loaded actuator for mechanical activation of membrane proteins.

A Mills, N Aissaoui, D Maurel, J Elezgaray, F Morvan, J J Vasseur, E Margeat, R B Quast, J Lai Kee-Him, N Saint and 4 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.7field-weighted citation impact, top 5% 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

22 citing papers in PubMed, 45 citations in OpenAlex.

  1. Article
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  5. Plasmonic Nano-bolas Hunt DNA Targets.ACS nanoscience Au · 2026
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  12. A DNA-Based Plasmonic Nano-Ruler.International journal of molecular sciences · 2025
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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

14 authors at 2 institutions in 1 country.

A MillsUniversité de Montpellier, Centre de Biochimie Structurale, INSERM, CNRS, 34090, Montpellier, France.
N AissaouiUniversité de Montpellier, Centre de Biochimie Structurale, INSERM, CNRS, 34090, Montpellier, France.ORCID http://orcid.org/0000-0002-0591-5934
D MaurelUniversité de Montpellier, Institut de Génomique Fonctionnelle, INSERM, CNRS, 34090, Montpellier, France.
J ElezgarayCRPP, CNRS, UMR 5031, Université de Bordeaux, Pessac, France.
F MorvanIBMM, Université de Montpellier, CNRS, ENSCM, Montpellier, France.ORCID http://orcid.org/0000-0001-5077-0028
J J VasseurIBMM, Université de Montpellier, CNRS, ENSCM, Montpellier, France.
E MargeatUniversité de Montpellier, Centre de Biochimie Structurale, INSERM, CNRS, 34090, Montpellier, France.ORCID http://orcid.org/0000-0001-6063-6420
R B QuastUniversité de Montpellier, Centre de Biochimie Structurale, INSERM, CNRS, 34090, Montpellier, France.ORCID http://orcid.org/0000-0001-8166-6952
J Lai Kee-HimUniversité de Montpellier, Centre de Biochimie Structurale, INSERM, CNRS, 34090, Montpellier, France.
N SaintPHYMEDEXP, Université de Montpellier, CNRS, INSERM, 34090, Montpellier, France.
C BenistantUniversité de Montpellier, Centre de Biochimie Structurale, INSERM, CNRS, 34090, Montpellier, France.
A NordUniversité de Montpellier, Centre de Biochimie Structurale, INSERM, CNRS, 34090, Montpellier, France.ORCID http://orcid.org/0000-0001-6199-2769
F PedaciUniversité de Montpellier, Centre de Biochimie Structurale, INSERM, CNRS, 34090, Montpellier, France.ORCID http://orcid.org/0000-0002-4530-3027
G BellotUniversité de Montpellier, Centre de Biochimie Structurale, INSERM, CNRS, 34090, Montpellier, France. gaetan.bellot@inserm.fr.
Centre National de la Recherche Scientifique · FRÉcole Nationale Supérieure de Chimie de Montpellier · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

How cells respond to mechanical forces by converting them into biological signals underlie crucial cellular processes. Our understanding of mechanotransduction has been hindered by technical barriers, including limitations in our ability to effectively apply low range piconewton forces to specific mechanoreceptors on cell membranes without laborious and repetitive trials. To overcome these challenges we introduce the Nano-winch, a robust, easily assembled, programmable DNA origami-based molecular actuator. The Nano-winch is designed to manipulate multiple mechanoreceptors in parallel by exerting fine-tuned, low- piconewton forces in autonomous and remotely activated modes via adjustable single- and double-stranded DNA linkages, respectively. Nano-winches in autonomous mode can land and operate on the cell surface. Targeting the device to integrin stimulated detectable downstream phosphorylation of focal adhesion kinase, an indication that Nano-winches can be applied to study cellular mechanical processes. Remote activation mode allowed finer extension control and greater force exertion. We united remotely activated Nano-winches with single-channel bilayer experiments to directly observe the opening of a channel by mechanical force in the force responsive gated channel protein, BtuB. This customizable origami provides an instrument-free approach that can be applied to control and explore a diversity of mechanotransduction circuits on living cells.

Indexed as

Mechanotransduction, CellularMembrane ProteinsDNAFocal Adhesion Protein-Tyrosine KinasesMechanoreceptorsStress, MechanicalDNAFocal Adhesion Protein-Tyrosine KinasesMembrane Proteins

Identifiers

PMID35902570
PMCPMC9334261
OpenAlexW4288427167

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.