Evidence map›Paper›PMID 40696880›Full record

ArticleACS applied materials & interfaces2025

Self-Assembling Aromatic Peptide Amphiphile Fibers for Multivalent Display of Enzymatically Linked Antigenic Proteins.

Rie Wakabayashi, Ghazian Dzaky Syahid Fathullah, Ayato Higuchi, Honggang Cui, Kosuke Minamihata, Noriho Kamiya, Masahiro Goto

Abstract read
In one paragraph

Article in ACS applied materials & interfaces, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

7 authors.

Rie WakabayashiDepartment of Applied Chemistry, Graduate School of Engineering, Kyushu University, Fukuoka 819-0395, Japan.ORCID 0000-0003-0348-8091
Ghazian Dzaky Syahid FathullahDepartment of Applied Chemistry, Graduate School of Engineering, Kyushu University, Fukuoka 819-0395, Japan.
Ayato HiguchiDepartment of Applied Chemistry, Graduate School of Engineering, Kyushu University, Fukuoka 819-0395, Japan.
Honggang CuiDepartment of Chemical and Biomolecular Engineering, and Institute for NanoBiotechnology, The Johns Hopkins University, Baltimore, Maryland 21218, United States.ORCID 0000-0002-4684-2655
Kosuke MinamihataDepartment of Applied Chemistry, Graduate School of Engineering, Kyushu University, Fukuoka 819-0395, Japan.
Noriho KamiyaDepartment of Applied Chemistry, Graduate School of Engineering, Kyushu University, Fukuoka 819-0395, Japan.ORCID 0000-0003-4898-6342
Masahiro GotoDepartment of Applied Chemistry, Graduate School of Engineering, Kyushu University, Fukuoka 819-0395, Japan.ORCID 0000-0002-2008-9351

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Supramolecular fibers assembled from peptide amphiphiles are promising materials for the delivery of biopharmaceuticals. However, strategies for directly conjugating folded proteins onto these supramolecular dynamic assemblies remain limited. Herein, we demonstrate that aromatic peptide amphiphiles that integrate self-assembly motifs with enzymatic recognition sequences enable the synthesis of supramolecular fibrous materials amenable to protein conjugation in their native folded state. The designed peptide amphiphiles self-assembled into fibers through a combination of hydrophobic, aromatic, and hydrogen bonding interactions in aqueous media. Using microbial transglutaminase, a recombinant enhanced green fluorescent protein (EGFP), used as a model proteinaceous antigen, was covalently coupled to the fibers via site-specific enzymatic cross-linking. This direct conjugation greatly enhanced the intracellular delivery of EGFP to murine dendritic cells in a manner dependent upon the peptide design. Notably, the resulting conjugates exhibited markedly increased immunogenicity compared to the protein alone, as evidenced by the elevated production of antigen-specific immunoglobulin G. These findings position the conjugated supramolecular fibers as a versatile platform for protein delivery and vaccine development.

Indexed as

AntigensGreen Fluorescent ProteinsPeptidesSurface-Active AgentsAnimalsDendritic CellsHydrophobic and Hydrophilic InteractionsMiceTransglutaminasesAntigensenhanced green fluorescent proteinGreen Fluorescent ProteinsPeptidesSurface-Active AgentsTransglutaminasesenzymatic reactionimmune materialintracellular protein deliverypeptide amphiphilesself-assembly

Identifiers

PMID40696880
PMCPMC12332845

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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.