Evidence map›Paper›PMID 39186653›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2024

Nucleated synthetic cells with genetically driven intercompartment communication.

Ion A Ioannou, Carolina Monck, Francesca Ceroni, Nicholas J Brooks, Marina K Kuimova, Yuval Elani

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Membrane-Associated Biomolecules for Synthetic Cell Signalling.Chembiochem : a European journal of chemical biology · 2026
    Review
  3. Article
  4. Article
  5. 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

6 authors.

Ion A IoannouDepartment of Chemistry, Imperial College London, Molecular Sciences Research Hub, London W12 0BZ, United Kingdom.ORCID 0000-0001-8749-1049
Carolina MonckDepartment of Chemical Engineering, Imperial College London, London SW7 2AZ, United Kingdom.
Francesca CeroniDepartment of Chemical Engineering, Imperial College London, London SW7 2AZ, United Kingdom.ORCID 0000-0001-7237-4982
Nicholas J BrooksDepartment of Chemistry, Imperial College London, Molecular Sciences Research Hub, London W12 0BZ, United Kingdom.
Marina K KuimovaDepartment of Chemistry, Imperial College London, Molecular Sciences Research Hub, London W12 0BZ, United Kingdom.
Yuval ElaniDepartment of Chemical Engineering, Imperial College London, London SW7 2AZ, United Kingdom.

Funding

UK Research and Innovation (UKRI) MR/S031537/1UKRI | Biotechnology and Biological Sciences Research Council (BBSRC) BB/W00125X/1
6 · The paper itself

Abstract

Eukaryotic cells are characterized by multiple chemically distinct compartments, one of the most notable being the nucleus. Within these compartments, there is a continuous exchange of information, chemicals, and signaling molecules, essential for coordinating and regulating cellular activities. One of the main goals of bottom-up synthetic biology is to enhance the complexity of synthetic cells by establishing functional compartmentalization. There is a need to mimic autonomous signaling between compartments, which in living cells, is often regulated at the genetic level within the nucleus. This advancement is key to unlocking the potential of synthetic cells as cell models and as microdevices in biotechnology. However, a technological bottleneck exists preventing the creation of synthetic cells with a defined nucleus-like compartment capable of genetically programmed intercompartment signaling events. Here, we present an approach for creating synthetic cells with distinct nucleus-like compartments that can encapsulate different biochemical mixtures in discrete compartments. Our system enables in situ protein expression of membrane proteins, enabling autonomous chemical communication between nuclear and cytoplasmic compartments, leading to downstream activation of enzymatic pathways within the cell.

Indexed as

Artificial CellsCell NucleusSynthetic BiologyCell CommunicationCytoplasmSignal Transductionartificial cellscell-free protein expressionmembranessynthetic biologyvesicles

Identifiers

PMID39186653
PMCPMC11388312

What OpenQuestion holds

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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.