| Literature DB >> 25815145 |
Soraya Z Ferreira1, Hellem C Carneiro1, Hugo A Lara1, Rosemeire B Alves1, Jarbas M Resende1, Heloísa M Oliveira2, Luciana M Silva2, Daniel A Santos1, Rossimiriam P Freitas1.
Abstract
Antimicrobial peptides (AMPs) are currently being investigated as potential sources of novel therapeutics against an increasing number of microorganisms resistant to conventional antibiotics. The conjugation of an AMP to other bioactive compounds is an interesting approach for the development of new derivatives with increased antimicrobial efficiency and broader spectra of action. In this work, the synthesis of a new peptide-coumarin conjugate via copper(I)-catalyzed azide-alkyne cycloaddition is described. The conjugate was assayed for in vitro cytotoxicity and displayed antifungal activity against Cryptococcus gattii and Cryptococcus neoformans. Additionally, the conjugate exhibited increased antifungal efficacy when compared with the individual peptide, coumarin, or triazole moieties. Treatment of C. gattii with the peptide-coumarin conjugate enhanced the production of reactive oxygen species, suggesting that the oxidative burst plays an important role in the mechanism of action of the conjugate.Entities:
Keywords: Antimicrobial peptide; copper(I)-catalyzed azide−alkyne cycloaddition; coumarin; cryptococcosis; reactive oxygen species
Year: 2015 PMID: 25815145 PMCID: PMC4360150 DOI: 10.1021/ml500393q
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345