Evidence map›Paper›PMID 41851244›Full record

ArticleCommunications biology2026

Riboswitch-controlled lipid conversion enables functional membrane asymmetry in artificial cells.

Koki Kamiya, Sumin Lee, Kotaro Baba

Abstract read
In one paragraph

Article in Communications biology, 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

3 authors.

Koki KamiyaGraduate School of Science and Technology, Gunma University, Gunma, Japan. kamiya@gunma-u.ac.jp.ORCID http://orcid.org/0000-0001-9143-9841
Sumin LeeGraduate School of Science and Technology, Gunma University, Gunma, Japan.
Kotaro BabaGraduate School of Science and Technology, Gunma University, Gunma, Japan.

Funding

MEXT | Japan Society for the Promotion of Science (JSPS) JP22H01874MEXT | Japan Society for the Promotion of Science (JSPS) JP24H00889
6 · The paper itself

Abstract

Dynamic regulation of lipid membrane composition is fundamental to living cells; however, synthetic analogs capable of such regulation remain scarce. Here, we present an artificial cell platform in which riboswitch-mediated expression of phospholipase D (PLD) enables stimulus-responsive lipid remodeling within lipid vesicles. In this system, chemically induced activation of a fluoride-responsive riboswitch triggers cell-free synthesis of PLD, which hydrolyzes phosphatidylcholine (PC) to phosphatidic acid (PA) in the inner leaflet of the vesicles. This enzymatic reaction generates a negatively charged asymmetric membrane, enabling functionalization with mechanosensitive channels such as the mechanosensitive channel of large conductance (MscL). We characterized the kinetics of asymmetry generation by varying plasmid DNA and fluoride concentrations, and evaluated membrane behavior using lipid compositions with or without cholesterol. Our platform demonstrates a strategy for coupling gene expression to dynamic membrane remodeling and underscores the potential of riboswitch-regulated lipid transitions in building environment-responsive artificial cells with programmable functions.

Indexed as

Artificial CellsCell MembraneMembrane LipidsRiboswitchPhosphatidic AcidsPhosphatidylcholinesPhospholipase DMembrane LipidsPhosphatidic AcidsPhosphatidylcholinesPhospholipase DRiboswitch

Identifiers

PMID41851244
PMCPMC13121617

What OpenQuestion holds

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LicenceCC BY
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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.