| Literature DB >> 20585128 |
Daniel Knappe1, Petra Henklein, Ralf Hoffmann, Kai Hilpert.
Abstract
Antimicrobial peptides are promising novel peptide leads, but their low serum stability often limits their further consideration in drug development programs. Here, we describe a generally applicable strategy to stabilize peptides against serum proteases by replacing arginine residues with alpha-amino-3-guanidino-propionic acid (Agp). Peptide NH(2)-RRWRIVVIRVRR-CONH(2) was nearby totally degraded after 8 h in mouse serum, whereas the variant with Agp substituted was degraded less than 20%. The antimicrobial activity was not affected.Entities:
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Year: 2010 PMID: 20585128 PMCID: PMC2934954 DOI: 10.1128/AAC.00300-10
Source DB: PubMed Journal: Antimicrob Agents Chemother ISSN: 0066-4804 Impact factor: 5.191