Evidence map›Paper›PMID 42246404›Full record

ArticleSmall (Weinheim an der Bergstrasse, Germany)2026

Self-Assembling Cationic Lipopeptides for the Construction of Functional Vesicular Gene-Delivery Systems.

Federica A Souto-Trinei, Alba Ramil-Bouzas, Paco Fernández-Trillo, Ana Rey-Rico, Roberto J Brea

Abstract read
In one paragraph

Article in Small (Weinheim an der Bergstrasse, Germany), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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.

Federica A Souto-TrineiBioinspired Nanochemistry (BioNanoChem) Group, CICA - Centro Interdisciplinar de Química e Bioloxía, Departamento de Química, Facultad de Ciencias, Universidade da Coruña, A Coruña, Spain.ORCID https://orcid.org/0000-0003-1785-6078
Alba Ramil-BouzasBioinspired Nanochemistry (BioNanoChem) Group, CICA - Centro Interdisciplinar de Química e Bioloxía, Departamento de Química, Facultad de Ciencias, Universidade da Coruña, A Coruña, Spain.ORCID https://orcid.org/0009-0000-2736-9228
Paco Fernández-TrilloBioinspired Nanochemistry (BioNanoChem) Group, CICA - Centro Interdisciplinar de Química e Bioloxía, Departamento de Química, Facultad de Ciencias, Universidade da Coruña, A Coruña, Spain.ORCID https://orcid.org/0000-0002-6680-5683
Ana Rey-RicoGene and Cell Therapy (G-CEL) Research Group, CICA - Centro Interdisciplinar de Química e Bioloxía, Departamento de Biología, Facultad de Ciencias, Universidade da Coruña, A Coruña, Spain.ORCID https://orcid.org/0000-0003-1682-498X
Roberto J BreaBioinspired Nanochemistry (BioNanoChem) Group, CICA - Centro Interdisciplinar de Química e Bioloxía, Departamento de Química, Facultad de Ciencias, Universidade da Coruña, A Coruña, Spain.ORCID https://orcid.org/0000-0002-0321-0156

Funding

Agencia Estatal de Investigación CNS2024-154660Agencia Estatal de Investigación PID2021-128113NA-I100Agencia Estatal de Investigación PID2021-128461OB-I00Agencia Estatal de Investigación RYC2020-030065-IConsellería de Cultura, Educación e Universidade da Xunta de Galicia ED431B 2023/60Consellería de Cultura, Educación e Universidade da Xunta de Galicia ED431F 2024/07
6 · The paper itself

Abstract

Delivering nucleic acids across cellular membranes remains a central challenge. Although synthetic gene carriers that mimic living cells are gaining interest, creating robust and biocompatible compartments continues to be technically demanding and limited in scope. Here, we present a new class of cationic lipopeptides that self-assemble into stable, functional membrane structures, offering a versatile platform for gene-delivery applications. These lipopeptides combine the biological activity and programmability of peptides with the self-organizing behavior of lipids, yielding functional vesicular structures that emulate cellular compartments and act as powerful non-viral vectors. We demonstrate that these assemblies efficiently sequester and deliver nucleic acids, achieving high transfection efficiency with minimal cytotoxicity in HEK 293T cells, and importantly, extending this performance to more challenging cellular models such as mesenchymal stem cells (MSCs). Our findings highlight the potential of self-assembling cationic lipopeptides as modular building blocks for generating robust, biocompatible, and programmable synthetic cells capable of delivering diverse nucleic acids.

Indexed as

Gene Transfer TechniquesLipopeptidesCationsHEK293 CellsHumansTransfectionCationsLipopeptidesgene deliverylipopeptideself‐assemblysynthetic cellvesicle

Identifiers

PMID42246404
PMCPMC13410438

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.