Evidence map›Paper›PMID 42007734›Full record

ArticleNano letters2026

Using DNA Origami to Study Nanoscale Organization of Plasma Membranes.

Eloina Corradi, Konlin Shen, Zeynep Karatas, Maureen Cercy, Thomas Schlichthaerle, Margaux Caumont, Mélissande Osouf, Brune Vialet, Philippe Barthelemy, Morgane Rosendale and 6 more

Abstract read
In one paragraph

Article in Nano letters, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors.

Eloina CorradiUniversity Bordeaux, CNRS, IINS, UMR 5297, Bordeaux, F-33000, France.
Konlin ShenDept. of Cellular and Molecular Pharmacology, University of California San Francisco, San Francisco, California 94158, United States.ORCID 0000-0003-1184-7605
Zeynep KaratasUniversity Bordeaux, CNRS, IINS, UMR 5297, Bordeaux, F-33000, France.
Maureen CercyUniversity Bordeaux, CNRS, IINS, UMR 5297, Bordeaux, F-33000, France.
Thomas SchlichthaerleFaculty of Physics and Center for Nanoscience, LMU Munich, Munich, 80539, Germany.
Margaux CaumontUniversity Bordeaux, CNRS, IINS, UMR 5297, Bordeaux, F-33000, France.
Mélissande OsoufUniversity Bordeaux, CNRS, IINS, UMR 5297, Bordeaux, F-33000, France.
Brune VialetARNA, INSERM U1212, CNRS 5320, Université de Bordeaux, Bordeaux, F-33076, France.
Philippe BarthelemyARNA, INSERM U1212, CNRS 5320, Université de Bordeaux, Bordeaux, F-33076, France.
Morgane RosendaleUniversity Bordeaux, CNRS, IINS, UMR 5297, Bordeaux, F-33000, France.
Adiyodi Veetil RadhakrishnanUniversity Bordeaux, CNRS, IINS, UMR 5297, Bordeaux, F-33000, France.
Tianchi ChenUniversity Bordeaux, CNRS, IINS, UMR 5297, Bordeaux, F-33000, France.
Ralf JungmannFaculty of Physics and Center for Nanoscience, LMU Munich, Munich, 80539, Germany.ORCID 0000-0003-4607-3312
Arnaud GissotARNA, INSERM U1212, CNRS 5320, Université de Bordeaux, Bordeaux, F-33076, France.ORCID 0000-0002-0942-9087
Shawn M DouglasDept. of Cellular and Molecular Pharmacology, University of California San Francisco, San Francisco, California 94158, United States.
Grégory GiannoneUniversity Bordeaux, CNRS, IINS, UMR 5297, Bordeaux, F-33000, France.ORCID 0000-0002-0932-1690

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Plasma membrane (PM) lipids and proteins partition into nanodomains that regulate cellular processes by controlling local membrane organization. However, nanodomains' small size and temporal instability hinder their study in living cells. To address this, we built fluorescent DNA origami probes that insert into the PM via lipid anchors displayed on cells. Using DNA origami allows precise control over anchor number and spatial arrangement, enabling nanometer-scale sampling of the PM. Once inserted, probes diffusing across the membrane are followed by single-particle tracking to survey the PM landscape. Varying lipid anchor number and arrangement shows that origami immobilization requires simultaneous interactions with multiple nanodomains. Disrupting the actin cytoskeleton reduced immobilization, confirming its role in nanodomain stability. Moreover, acute cell stretching transiently increases origami mobility, indicating that mechanical forces can reversibly regulate PM nanodomain organization. This novel membrane-integrated DNA origami approach provides mechanistic insights into PM nanodomain architecture and dynamics in living cells.

Indexed as

Cell MembraneDNADNA NanostructuresActin CytoskeletonFluorescent DyesHumansDNAFluorescent Dyesactin cytoskeletonDNA origamimechanobiologyplasma membrane nanodomainssingle particle tracking

Identifiers

PMID42007734
PMCPMC13329991

What OpenQuestion holds

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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.