Evidence map›Paper›PMID 39805958›Full record

ArticleNature materials2025

Morphology remodelling and membrane channel formation in synthetic cells via reconfigurable DNA nanorafts.

Sisi Fan, Shuo Wang, Longjiang Ding, Thomas Speck, Hao Yan, Stephan Nussberger, Na Liu

Abstract read
In one paragraph

Article in Nature materials, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Controlling membrane tension by dynamic DNA nanorings.bioRxiv : the preprint server for biology · 2026
    Article
  6. Review
  7. Article
  8. Article
  9. Plasmonic Nano-bolas Hunt DNA Targets.ACS nanoscience Au · 2026
    Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Article
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

7 authors.

Sisi Fan *2nd Physics Institute, University of Stuttgart, Stuttgart, Germany.
Shuo Wang *Department of Biophysics, Institute of Biomaterials and Biomolecular Systems, University of Stuttgart, Stuttgart, Germany.ORCID 0000-0003-1107-9597
Longjiang Ding *2nd Physics Institute, University of Stuttgart, Stuttgart, Germany.
Thomas SpeckInstitute for Theoretical Physics IV, University of Stuttgart, Stuttgart, Germany.
Hao YanBiodesign Center for Molecular Design and Biomimetics, Arizona State University, Tempe, AZ, USA. hao.yan@asu.edu.ORCID 0000-0001-7397-9852
Stephan NussbergerDepartment of Biophysics, Institute of Biomaterials and Biomolecular Systems, University of Stuttgart, Stuttgart, Germany. stephan.nussberger@bio.uni-stuttgart.de.ORCID 0000-0003-3619-4452
Na Liu2nd Physics Institute, University of Stuttgart, Stuttgart, Germany. na.liu@pi2.uni-stuttgart.de.ORCID 0000-0001-5831-3382

Funding

Alexander von Humboldt-Stiftung (Alexander von Humboldt Foundation) Humboldt Research AwardBaden-Württemberg Stiftung (Baden-Württemberg Foundation) BWST-ISF2020-19Deutsche Forschungsgemeinschaft (German Research Foundation) 431314977/GRK2642Max-Planck-Gesellschaft (Max Planck Society) Max Planck Fellow
6 · The paper itself

Abstract

The shape of biological matter is central to cell function at different length scales and determines how cellular components recognize, interact and respond to one another. However, their shapes are often transient and hard to reprogramme. Here we construct a synthetic cell model composed of signal-responsive DNA nanorafts, biogenic pores and giant unilamellar vesicles (GUVs). We demonstrate that reshaping of DNA rafts at the nanoscale can be coupled to reshaping of GUVs at the microscale. The nanorafts collectively undergo reversible transitions between isotropic and short-range local order on the lipid membrane, programmably remodelling the GUV shape. Assisted by the biogenic pores, during GUV shape recovery the locally ordered DNA rafts perforate the membrane, forming sealable synthetic channels for large cargo transport. Our work outlines a versatile platform for interfacing reconfigurable DNA nanostructures with synthetic cells, expanding the potential of DNA nanotechnology in synthetic biology.

Indexed as

Artificial CellsDNANanostructuresNanotechnologySynthetic BiologyUnilamellar LiposomesDNAUnilamellar Liposomes

Identifiers

PMID39805958
PMCPMC11790494

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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.