Evidence map›Paper›PMID 42209497›Full record

ArticleNature communications2026

Breaking the membrane heredity paradox through de novo protocell formation.

Satyam Khanal, Alessandro Fracassi, Alexander Harjung, Michael D Burkart, Neal K Devaraj

Abstract read
In one paragraph

Article in Nature communications, 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

5 authors.

Satyam Khanal *Department of Chemistry and Biochemistry, University of California, San Diego, CA, USA.
Alessandro Fracassi *Department of Chemistry and Biochemistry, University of California, San Diego, CA, USA.ORCID http://orcid.org/0000-0003-1239-6527
Alexander HarjungDepartment of Chemistry and Biochemistry, University of California, San Diego, CA, USA.ORCID http://orcid.org/0009-0002-4219-4686
Michael D BurkartDepartment of Chemistry and Biochemistry, University of California, San Diego, CA, USA. mburkart@ucsd.edu.ORCID http://orcid.org/0000-0002-4472-2254
Neal K DevarajDepartment of Chemistry and Biochemistry, University of California, San Diego, CA, USA. ndevaraj@ucsd.edu.ORCID http://orcid.org/0000-0002-8033-9973

Funding

NSF | BIO | Division of Molecular and Cellular Biosciences (MCB) MCB-2124105
6 · The paper itself

Abstract

Lipid membranes define cell boundaries, acting as gatekeepers for transport and signaling. A central paradigm in biology is that all cellular membranes descend from a common ancestral membrane, as they cannot be generated in the absence of pre-existing lipid structures. It is thus unclear whether lipid membranes can arise from membrane-less precursors. Here we demonstrate the de novo generation of lipid bilayers in the absence of any pre-existing membranes, membrane-bound proteins, or lipid nanostructure templates. Using acetate and cysteine as simple metabolites, lipid tails are constructed by soluble enzymes and spontaneously form diacyl lipids that assemble into vesicles. Pore-forming peptides facilitate precursor transport into vesicles, allowing the continuous generation of new lipids. Formation of glycolipid membranes creates compartments that can maintain proton gradients. Our findings demonstrate that lipid compartments can form without pre-existing membranes, establishing a unique route linking lipid synthesis to compartment formation and function.

Indexed as

Artificial CellsCell MembraneLipid BilayersMembrane LipidsLipid BilayersMembrane Lipids

Identifiers

PMID42209497
PMCPMC13388977

What OpenQuestion holds

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LicenceCC BY
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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.