| Literature DB >> 34203919 |
Carlo Diaferia1, Elisabetta Rosa1, Enrico Gallo2, Giovanni Smaldone2, Mariano Stornaiuolo1, Giancarlo Morelli1, Antonella Accardo1.
Abstract
Peptide-based hydrogels (PHGs) are biocompatible materials suitable for biological, biomedical, and biotechnological applications, such as drug delivery and diagnostic tools for imaging. Recently, a novel class of synthetic hydrogel-forming amphiphilic cationic peptides (referred to as series K), containing an aliphatic region and a Lys residue, was proposed as a scaffold for bioprinting applications. Here, we report the synthesis of six analogues of the series K, in which the acetyl group at the N-terminus is replaced by aromatic portions, such as the Fmoc protecting group or the Fmoc-FF hydrogelator. The tendency of all peptides to self-assemble and to gel in aqueous solution was investigated using a set of biophysical techniques. The structural characterization pointed out that only the Fmoc-derivatives of series K keep their capability to gel. Among them, Fmoc-K3 hydrogel, which is the more rigid one (G' = 2526 Pa), acts as potential material for tissue engineering, fully supporting cell adhesion, survival, and duplication. These results describe a gelification process, allowed only by the correct balancing among aggregation forces within the peptide sequences (e.g., van der Waals, hydrogen bonding, and π-π stacking).Entities:
Keywords: Fmoc peptides; peptide hydrogel; peptide materials; self-assembling; tissue engineering
Year: 2021 PMID: 34203919 DOI: 10.3390/biomedicines9060678
Source DB: PubMed Journal: Biomedicines ISSN: 2227-9059