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Fmoc-Phe: Fmoc-Leu supramolecular hydrogels with adaptive antibacterial activity

Chevigny, Romain, Rahkola, Henna, Sitsanidis, Efstratios D., kumpulainen, T, White, Lisa J., sundberg, L, Hiscock, Jennifer R., Pettersson, Mika, Nissinen, Maija (2026) Fmoc-Phe: Fmoc-Leu supramolecular hydrogels with adaptive antibacterial activity. RSC Advances, 16 (15). pp. 13801-13811. ISSN 2046-2069. (doi:10.1039/D5RA08809G) (KAR id:113371)

Abstract

The development of adaptive soft materials offers new opportunities to address the effects of antimicrobial resistance. Fmoc-phenylalanine (Fmoc-Phe) and Fmoc-leucine (Fmoc-Leu) based hydrogels are known to demonstrate antibacterial activity. We now show that by combining these two gelators (Fmoc-Phe and Fmoc-Leu) into a multicomponent hydrogel system, we can tune the antibacterial properties of the resultant hydrogel. This tunable antimicrobial behaviour is achieved by varying the Fmoc-Phe: Fmoc-Leu ratio, which also influences self-assembly and, as a result, the physical properties of the material. We show that changing the component ratio can be used to optimise gelation efficiency and modulate viscoelastic, self-healing and thermoresponsive properties. Spectroscopic analyses reveal that while β-sheet organisation is retained independently of the ratio of gelators supplied, system stability (increasing material softness) is observed as a direct result of the proportion of the gelator that remains unassembled in the sol of the resultant hydrogel. Antibacterial assays conducted against clinically relevant Gram-positive and Gram-negative pathogens demonstrate formulation-dependent responses, with Gram-positive strains showing the greatest susceptibility. From these data, we can determine a structure–activity relationship, which demonstrates the importance of compositional tuning as a simple and effective strategy for designing peptide-based hydrogels with tailorable physical, material and antimicrobial properties.

Item Type: Article
DOI/Identification number: 10.1039/D5RA08809G
Subjects: Q Science
Q Science > QD Chemistry
Q Science > QD Chemistry > QD431 Organic Chemistry- Biochemistry- Proteins, peptides, amino acids
Institutional Unit: Schools > School of Natural Sciences
Schools > School of Natural Sciences > Chemistry and Forensic Science
Former Institutional Unit:
There are no former institutional units.
Funders: UK Research and Innovation (https://ror.org/001aqnf71)
Depositing User: Jennifer Hiscock
Date Deposited: 10 Mar 2026 11:40 UTC
Last Modified: 25 Mar 2026 03:51 UTC
Resource URI: https://kar.kent.ac.uk/id/eprint/113371 (The current URI for this page, for reference purposes)

University of Kent Author Information

Sitsanidis, Efstratios D..

Creator's ORCID:
CReDIT Contributor Roles:

Hiscock, Jennifer R..

Creator's ORCID: https://orcid.org/0000-0002-1406-8802
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