Evidence map›Paper›PMID 40370199›Full record

ArticleChemistry (Weinheim an der Bergstrasse, Germany)2025

Hybrid pH Responsive Supramolecular Polymers Through the Combination of the Ureido-Pyrimidinone Motif with β-Sheet Peptide Sequences.

Riccardo Bellan, David Attia, Marcel H P van Genderen, Patricia Y W Dankers

Abstract read
In one paragraph

Article in Chemistry (Weinheim an der Bergstrasse, Germany), 2025. 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

4 authors.

Riccardo BellanInstitute for Complex Molecular Systems and Department of Biomedical Engineering, Eindhoven University of Technology, 5600 MB, Eindhoven, The Netherlands.ORCID https://orcid.org/0009-0002-3196-979X
David AttiaInstitute for Complex Molecular Systems and Department of Biomedical Engineering, Eindhoven University of Technology, 5600 MB, Eindhoven, The Netherlands.
Marcel H P van GenderenInstitute for Complex Molecular Systems and Department of Biomedical Engineering, Eindhoven University of Technology, 5600 MB, Eindhoven, The Netherlands.
Patricia Y W DankersInstitute for Complex Molecular Systems and Department of Biomedical Engineering, Eindhoven University of Technology, 5600 MB, Eindhoven, The Netherlands.

Funding

European Union's Horizon research and innovation program 101079482HORIZON EUROPE Framework Programme 101079482Ministerie van Onderwijs, Cultuur en Wetenschap 024.005.020Ministry of Education, Culture and Science 024.005.020Nederlandse Organisatie voor Wetenschappelijk Onderzoek VI.C.222.088Netherlands Organization for Scientific Research VI.C.222.088
6 · The paper itself

Abstract

Supramolecular biomaterials based on 1D supramolecular polymers in water replicate the fibrous and dynamic structures of natural architectures. Peptides, valued for their biocompatibility, are commonly employed as building blocks for supramolecular biomaterials, often in combination with large aromatic or hydrogen-bonding groups at the N-terminus to improve their structural stability. Herein, the self-assembly properties of two β-sheet peptides combined with the ureido-pyrimidinone self-dimerizing motif in aqueous solution are investigated in detail. The assembly of the resulting molecules is demonstrated to be intimately dependent on the β-sheet sequence, while the incorporation of a hydrophobic spacer enhances the assembly of the monomers, irrespective of the peptide sequence employed. Furthermore, the assembly of each monomer is significantly enhanced at pH = 3.0 while being stable between pH = 5.0 and 9.0. Only at pH = 12, upon enolate formation, the transition to random coil conformation is observed for all the monomers. The supramolecular polymers developed hereby point to fundamental design principle toward the development of UPy-peptide based materials with tuneable properties and potential applications in the biomedical fields of research.

Indexed as

PeptidesPolymersPyrimidinonesUreaAmino Acid SequenceHydrogen BondingHydrogen-Ion ConcentrationHydrophobic and Hydrophilic InteractionsProtein Conformation, beta-StrandPeptidesPolymersPyrimidinonesUreaassemblieshydrogen bonding unitpeptidessupramolecular chemistry

Identifiers

PMID40370199
PMCPMC12160978

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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.