| Literature DB >> 31532989 |
Franziska Clauder1, Anne Sophie Czerniak1, Sabrina Friebe2, Stefan G Mayr2, Dierk Scheinert3, Annette G Beck-Sickinger1.
Abstract
Common interventional therapies for cardiovascular occlusive diseases, such as the implantation of stents, are at risk of complications like thrombosis or restenosis. Drug-eluting stents have improved patency but simultaneously worsen the endothelialization of the implant. Here, we present a novel peptide coating derived from three proteins of the extracellular matrix named fibronectin, laminin, and elastin. Their active sequences RGD, SIKVAV, and VGVAPG were immobilized onto titanium surfaces by a carrier peptide containing l-3,4-dihydroxyphenylalanine (DOPA). Simultaneous functionalization of the carrier peptide with cyclic c[RGDfK] and SIKVAV had the most potent influence on adhesion, proliferation, viability, and angiogenesis of endothelial cells. By presentation of two adhesion peptides in one molecule, a synergistic enhancement of cell-surface interactions was achieved. Overall, this work clearly demonstrates the advantages of spatially defined peptide coatings for the endothelialization of titanium and thus describes a promising approach for the coating of stents.Entities:
Year: 2019 PMID: 31532989 DOI: 10.1021/acs.bioconjchem.9b00573
Source DB: PubMed Journal: Bioconjug Chem ISSN: 1043-1802 Impact factor: 4.774