Solid-Phase Synthesis of Reactive Peptide Crosslinker by Selective Deprotection

Title: Solid-Phase Synthesis of Reactive Peptide Crosslinker by Selective Deprotection

Volume: 13 Issue: 7

Author(s): Xuezhong He and Esmaiel Jabbari

Affiliation:

Keywords: Reactive peptide, functionalization, selective deprotection, solid-phase, enzymatic degradation, biomimetic crosslinker

Abstract: An effective and simple strategy for preparing peptide crosslinkers is described. An MMP-13 degradable peptide QPQGLAK-NH2 was prepared on the solid-phase using Fmoc chemistry. The peptide crosslinker was synthesized onbead by the coupling reaction between acrylic acid and the amine groups of glutamine and lysine residues. The synthetic procedure employed the acid-labile Fmoc-Lys (Mtt)-OH and base-labile Fmoc-AA-OH derivatives. Selective deprotection, of – Mtt and -Fmoc groups on-bead, freed the amine end-groups on glutamine and lysine residues for coupling reaction with acrylic acid while maintaining the peptide attached to the resin. Subsequent cleavage from the resin yielded a peptide crosslinker with two unsaturated acrylate end-groups with high yield and purity. This method can be generally employed for the synthesis of a wide range of peptides with one or more reactive groups for grafting in the fabrication of biomimetic scaffolds in tissue engineering applications.

Cite this article as:

He Xuezhong and Jabbari Esmaiel, Solid-Phase Synthesis of Reactive Peptide Crosslinker by Selective Deprotection, Protein & Peptide Letters 2006; 13 (7) . https://dx.doi.org/10.2174/092986606777790610

DOI https://dx.doi.org/10.2174/092986606777790610	Print ISSN 0929-8665
Publisher Name Bentham Science Publisher	Online ISSN 1875-5305