Lipidated α-Peptide/β-Peptoid Hybrids with Potent Anti-inflammatory Activity

Research output: Contribution to journalJournal articleResearchpeer-review

Sarah Line Skovbakke, Camilla Josephine Larsen, Peter Mikael Helweg Heegaard, Lise Moesby, Henrik Franzyk

In this study we investigated, optimized, and characterized a novel subclass of host defense peptide (HDP) mimics based on α-peptide/β-peptoid hybrid oligomers with an alternating cationic/hydrophobic design with respect to their ability to modulate the pro-inflammatory response by human primary leukocytes upon exposure to bacterial components. Structure-activity studies revealed that certain lipidated α-peptide/β-peptoid hybrid oligomers possess anti-inflammatory activities in the submicromolar range with low cytotoxicity, and that the anti-inflammatory activity of the HDP mimics is dependent on the length and position of the lipid element(s). The resulting lead compound, Pam-(Lys-βNSpe)6-NH2, blocks LPS-induced cytokine secretion with a potency comparable to that of polymyxin B. The mode of action of this HDP mimic does not involve direct LPS interaction since it, in contrast to polymyxin B, displayed only minor activity in the Limulus amebocyte lysate assay. Flow cytometry data showed specific interaction of a fluorophore-labeled lipidated α-peptide/β-peptoid hybrid with monocytes and granulocytes indicating a cellular target expressed by these leukocyte subsets.

Original languageEnglish
JournalJournal of Medicinal Chemistry
Volume58
Issue number2
Pages (from-to)801-813
Number of pages13
ISSN0022-2623
DOIs
Publication statusPublished - 2015

ID: 129418778