Modular Tunable α-Helical Peptide Hydrogels for Neuronal Cells

D. Arne Scott, Alexandra Wasmuth, Edgardo Abelardo, Kieran L. Hudson, Andrew R. Thomson, Martin A. Birchall, Nazia Mehrban, Jeremy M. Henley, Derek N. Woolfson

Research output: Contribution to journalArticlepeer-review

Abstract

The assembly of synthetic modules into user-defined hydrogels for cell culture and clinical applications carries significant advantages over naturally derived materials. Modularity is exploited in synthetic-polymer-based hydrogels to alter their physical properties, and spatiotemporally incorporate signaling peptides and growth factors. By contrast, the design of self-assembling peptide hydrogels has focused largely on assessing cellular responses to unmodified hydrogels and introducing small cell-adhesive ligands. In short, the modularity of peptide hydrogels is yet to be fully exploited. Previously, hydrogelating self-assembling fibers (hSAFs) are reported in which two de novo designed α-helical peptides form gels when mixed. Here, rational peptide design and engineering are used to alter the elastic properties of these hydrogels, to introduce adhesion peptides and growth factors, and to spatially pattern proteins within them. Analysis of the viability and morphology of primary rat neurons cultured on these hydrogels indicates that the modularity of the hSAF system provides a flexible platform for manipulating cell behavior, with potential future applications for modeling natural systems in vitro and regenerative medicine in vivo.
Original languageEnglish
Article number2410333
JournalAdvanced Functional Materials
Volume35
Issue number1
Early online date24 Nov 2024
DOIs
Publication statusPublished - 2 Jan 2025

Data Availability Statement

The data that support the findings of this study are available from the corresponding author upon reasonable request.

Funding

The authors thank the University of Bristol School of Chemistry Mass Spectrometry Facility for access to the EPSRC\u2010funded Bruker Ultraflex MALDI\u2010TOF instrument (EP/K03927X/1) and BrisSynBio for access to the CEM Liberty Blue peptide synthesizer and the BMG Labtech Clariostar plate reader (BB/L01386X/1). The authors thank Mark Howarth for providing an expression vector containing the SpyCatcher sequence. Fluorescence and electron microscopy images were collected in the Wolfson Bioimaging facility at The University of Bristol. Photopatterning was performed using a mask aligner provided by the School of Physics, University of Bristol. Rheology measurements were collected using a rheometer provided by the School of Chemistry. This work was supported by the Biotechnology and Biological Sciences Research Council\u2010funded South West Biosciences Doctoral Training Partnership (training grant reference: BB/J014400/1 and BB/M009122/1).

FundersFunder number
Biotechnology and Biological Sciences Research Council‐funded South West BiosciencesBB/J014400/1, BB/M009122/1

    Keywords

    • de novo
    • hydrogels
    • peptide
    • regenerative medicine
    • self-assembling hydrogels

    ASJC Scopus subject areas

    • Electronic, Optical and Magnetic Materials
    • General Chemistry
    • Biomaterials
    • General Materials Science
    • Condensed Matter Physics
    • Electrochemistry

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