Facile Control over the Supramolecular Ordering of Self-assembled Peptide Scaffolds by Simultaneous Assembly with a Polysacharride.
Identifieur interne : 000956 ( PubMed/Curation ); précédent : 000955; suivant : 000957Facile Control over the Supramolecular Ordering of Self-assembled Peptide Scaffolds by Simultaneous Assembly with a Polysacharride.
Auteurs : Rui Li [Australie] ; Mitchell Boyd-Moss [Australie] ; Benjamin Long [Australie] ; Anne Martel [France] ; Andrew Parnell [Royaume-Uni] ; Andrew J C. Dennison [Royaume-Uni] ; Colin J. Barrow [Australie] ; David R. Nisbet [Australie] ; Richard J. Williams [Australie]Source :
- Scientific reports [ 2045-2322 ] ; 2017.
Abstract
Enabling control over macromolecular ordering and the spatial distribution of structures formed via the mechanisms of molecular self-assembly is a challenge that could yield a range of new functional materials. In particular, using the self-assembly of minimalist peptides, to drive the incorporation of large complex molecules will allow a functionalization strategy for the next generation of biomaterial engineering. Here, for the first time, we show that co-assembly with increasing concentrations of a highly charged polysaccharide, fucoidan, the microscale ordering of Fmoc-FRGDF peptide fibrils and subsequent mechanical properties of the resultant hydrogel can be easily and effectively manipulated without disruption to the nanofibrillar structure of the assembly.
DOI: 10.1038/s41598-017-04643-3
PubMed: 28684767
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<front><div type="abstract" xml:lang="en">Enabling control over macromolecular ordering and the spatial distribution of structures formed via the mechanisms of molecular self-assembly is a challenge that could yield a range of new functional materials. In particular, using the self-assembly of minimalist peptides, to drive the incorporation of large complex molecules will allow a functionalization strategy for the next generation of biomaterial engineering. Here, for the first time, we show that co-assembly with increasing concentrations of a highly charged polysaccharide, fucoidan, the microscale ordering of Fmoc-FRGDF peptide fibrils and subsequent mechanical properties of the resultant hydrogel can be easily and effectively manipulated without disruption to the nanofibrillar structure of the assembly.</div>
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