ArticleSmall (Weinheim an der Bergstrasse, Germany)2026
Self-Assembling Cationic Lipopeptides for the Construction of Functional Vesicular Gene-Delivery Systems.
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.
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.
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.
Who cites it
1 citing paper in PubMed.
- Bioorthogonal chemistry for deciphering lipid biology in living systems.RSC chemical biology · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
5 authors.
Funding
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.
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Registered trials
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.