AI Article Synopsis

  • Peptide-based hydrogels (PHGs) are versatile and biocompatible materials used in drug delivery and diagnostics, with a focus on a new class called series K, made from amphiphilic cationic peptides.
  • Recent research involved synthesizing six variants of series K by replacing the N-terminus acetyl group with aromatic components, analyzing their ability to self-assemble and form gels in water.
  • Among these, Fmoc-K3 emerged as the most promising gel, showing high rigidity and supporting cell functions, highlighting the importance of molecular interactions for its gelification process.

Article 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).

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8232644PMC
http://dx.doi.org/10.3390/biomedicines9060678DOI Listing

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