Evidence map›Paper›PMID 40577602›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2025

Designing Tunable DNA Condensates to Control Membrane Budding Transformation in Synthetic Cells.

Nastasja Kaletta, Sophia Burick, Yusuf Qudbuddin, Petra Schwille

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Membrane-Associated Biomolecules for Synthetic Cell Signalling.Chembiochem : a European journal of chemical biology · 2026
    Review
  3. Let There be Light! Light as an Engine and Regulator in Synthetic Cells.Angewandte Chemie (International ed. in English) · 2026
    Review
  4. Article
  5. Article
  6. 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

4 authors.

Nastasja KalettaDepartment of Cellular and Molecular Biophysics, Max Planck Institute of Biochemistry, Am Klopferspitz 18, 82152, Martinsried, Germany.ORCID https://orcid.org/0009-0009-3890-5642
Sophia BurickDepartment of Cellular and Molecular Biophysics, Max Planck Institute of Biochemistry, Am Klopferspitz 18, 82152, Martinsried, Germany.
Yusuf QudbuddinDepartment of Cellular and Molecular Biophysics, Max Planck Institute of Biochemistry, Am Klopferspitz 18, 82152, Martinsried, Germany.ORCID https://orcid.org/0000-0003-0054-0608
Petra SchwilleDepartment of Cellular and Molecular Biophysics, Max Planck Institute of Biochemistry, Am Klopferspitz 18, 82152, Martinsried, Germany.ORCID https://orcid.org/0000-0002-6106-4847

Funding

Deutsche Forschungsgemeinschaft Project M.MC.A.BIOC8019European Research Council (ERC) Synergy Grant MetaDivide 101167181HORIZON EUROPE Marie Sklodowska-Curie Actions 859416
6 · The paper itself

Abstract

Wetting interactions between biomolecular condensates and lipid membranes have demonstrated great potential to induce large-scale membrane transformations in synthetic cells. However, the ability to functionalize existing condensates and control their interactions with membranes is limited, restricting their utility in engineering controlled wetting behavior. Here, fully programmable condensates based on DNA Y-motifs are introduced to engineer precisely tunable wetting behavior. In contrast to unmodified condensates that show no interaction with membranes, wetting of supported lipid bilayers (SLBs) can be induced by partial cholesterol-functionalization of DNA nanostructures. Incorporating photoactivatable DNA-lipid linker enables contact angles to be controlled over a wide range by varying UV exposure times. Furthermore, selective partitioning of small unilamellar vesicles (SUVs) into DNA condensates is demonstrated via programmable surface interactions. In giant unilamellar vesicles (GUVs), membrane wetting of enclosed condensates can be efficiently induced post-fabrication and results in outward budding. Thus, this work establishes programmable DNA condensates as a powerful platform for fine-tuned control over membrane-associated processes in synthetic cells, exceeding traditional approaches such as altering lipid composition or environmental conditions. Finally, the platform provides the possibility to design smart drug carriers for controlled substance delivery and release, and represents a customizable model to study condensate-membrane dynamics.

Indexed as

Artificial CellsBiomolecular CondensatesDNALipid BilayersNanostructuresUnilamellar LiposomesWettabilityDNALipid BilayersUnilamellar LiposomesbuddingDNA nanotechnologyGUV shape transitionsliquid‐liquid phase separationmembrane biophysicsmembrane deformations

Identifiers

PMID40577602
PMCPMC12376574

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.