Evidence map›Paper›PMID 42677531›Full record

ArticleJournal of the American Chemical Society2026

Elucidating the Reciprocal Interplay between Supramolecular Polymer Cytoskeletons and Fuel-Dependent Synthetic Cells.

Nils Bäumer, Leonie Kauling, Benedikt Kirmayer, Simone M Poprawa, Arthur Neuberger, Job Boekhoven

Abstract read
In one paragraph

Article in Journal of the American Chemical Society, 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

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

6 authors.

Nils BäumerDepartment of Bioscience, School of Natural Sciences, Technical University of Munich, Lichtenbergstrasse 4, 85748Garching, Germany.ORCID 0009-0006-4095-7474
Leonie KaulingDepartment of Bioscience, School of Natural Sciences, Technical University of Munich, Lichtenbergstrasse 4, 85748Garching, Germany.
Benedikt KirmayerWalther-Straub-Institute of Pharmacology and Toxicology, LMU Medizin, Ludwig-Maximilians-Universität München, Goethestrasse 33, 80336Munich, Germany.
Simone M PoprawaDepartment of Bioscience, School of Natural Sciences, Technical University of Munich, Lichtenbergstrasse 4, 85748Garching, Germany.ORCID 0009-0000-8978-1242
Arthur NeubergerWalther-Straub-Institute of Pharmacology and Toxicology, LMU Medizin, Ludwig-Maximilians-Universität München, Goethestrasse 33, 80336Munich, Germany.
Job BoekhovenDepartment of Bioscience, School of Natural Sciences, Technical University of Munich, Lichtenbergstrasse 4, 85748Garching, Germany.ORCID 0000-0002-9126-2430

Funding

Alexander von Humboldt-Stiftung NABayerisches Staatsministerium f?r Wissenschaft und Kunst NAElitenetzwerk Bayern NAEuropean Commission 101124380European Commission 852187Max-Planck-Gesellschaft NAStudienstiftung des Deutschen Volkes NA
6 · The paper itself

Abstract

Synthetic cells are compartments designed to mimic the functions and characteristics of living cells. By constructing synthetic cells from abiotic, basic components (bottom-up), it is possible to investigate the minimal requirements for life and gain insights into fundamental principles of biology. Among the available platforms, complex coacervates are particularly attractive, due to their potential to encapsulate a wide range of biomolecules and other cargo, enabling genotype-phenotype mapping. By coupling coacervate formation to a fueled chemical reaction cycle, the synthetic cells become fuel-dependent, growing in the presence of fuel and decaying in its absence, resembling biological cells. However, constructing cellular substructures for these fuel-dependent synthetic cells, such as cytoskeletons, has remained an unresolved challenge. Here, we show that supramolecular (co)polymers can act as cytoskeletons for the synthetic cells, depending on their condenophilicity (their affinity for the droplet phase). By using two distinct supramolecular building blocks, the condenophilicity can be modulated. Supramolecular copolymers where only some of the monomers bind to the complex coacervate result in the formation of a protruding cytoskeleton in and around the droplet. However, as condenophilicity increases, the polymers partition strongly into the coacervates, leading to the formation of a fully encapsulated cytoskeleton. We found that these internal structures influence the synthetic cell properties, such as morphology and lifespan. Moreover, the synthetic cells can dynamically reconstitute the supramolecular fibers, creating distinct populations within the cells and the surrounding dilute phase. Our results demonstrate that orthogonally assembled structures can serve as cellular substructures for active complex coacervate-based synthetic cells, broadening the existing arsenal of tools to bestow these rudimentary synthetic cells with more life-like properties.

Indexed as

Artificial CellsCytoskeletonPolymersMacromolecular SubstancesMacromolecular SubstancesPolymers

Identifiers

PMID42677531
PMCPMC13523708

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.