Host-Guest-Mediated Epitope Presentation on Self-Assembled Peptide Amphiphile Hydrogels.

adamantane attachment bioactivity cyclodextrin noncovalent self-assembly

Journal

ACS biomaterials science & engineering
ISSN: 2373-9878
Titre abrégé: ACS Biomater Sci Eng
Pays: United States
ID NLM: 101654670

Informations de publication

Date de publication:
14 09 2020
Historique:
entrez: 18 1 2021
pubmed: 19 1 2021
medline: 15 5 2021
Statut: ppublish

Résumé

A key feature in biomaterial design is the incorporation of bioactive signals into artificial constructs to stimulate tissue regeneration. Most currently used hydrogel cell culture systems depend on the covalent attachment of extracellular matrix (ECM)-derived peptides to either macromolecular units or smaller self-assembling building blocks, thereby restricting biosignal presentation and adaptability. However, new ways to rationally incorporate adhesion epitopes through noncovalent interactions would offer opportunities to better recreate the dynamic and reversible nature of the native ECM. Here, we report on a noncovalent epitope presentation approach mediated by host-guest interactions. Using peptide amphiphile hydrogels, we demonstrate that the adamantane/β-cyclodextrin pair can be used to anchor RGDS cell adhesion signals onto self-assembled hydrogels

Identifiants

pubmed: 33455284
doi: 10.1021/acsbiomaterials.0c00549
doi:

Substances chimiques

Epitopes 0
Hydrogels 0
Peptides 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

4870-4880

Subventions

Organisme : Medical Research Council
ID : MR/R015651/1
Pays : United Kingdom

Auteurs

Carlos Redondo-Gómez (C)

School of Engineering & Materials Science, Queen Mary University of London, London E1 4NS, U.K.
Institute of Bioengineering, Queen Mary University of London, London E1 4NS, U.K.

Soraya Padilla-Lopategui (S)

School of Engineering & Materials Science, Queen Mary University of London, London E1 4NS, U.K.
Institute of Bioengineering, Queen Mary University of London, London E1 4NS, U.K.

Helena S Azevedo (HS)

School of Engineering & Materials Science, Queen Mary University of London, London E1 4NS, U.K.
Institute of Bioengineering, Queen Mary University of London, London E1 4NS, U.K.

Alvaro Mata (A)

School of Engineering & Materials Science, Queen Mary University of London, London E1 4NS, U.K.
Institute of Bioengineering, Queen Mary University of London, London E1 4NS, U.K.
School of Pharmacy, University of Nottingham, University Park, Nottingham NG7 2RD, U.K.
Department of Chemical and Environmental Engineering, University of Nottingham, University Park, Nottingham NG7 2RD, U.K.
Biodiscovery Institute, University of Nottingham, University Park, Nottingham NG7 2RD, U.K.

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Classifications MeSH