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Antifungal activity of C3a and C3a-derived peptides against Candida
Authors:Andreas Sonesson  Lovisa Ringstad  Martin Malmsten  Artur Schmidtchen
Institution:a Department of Clinical Sciences, Section of Dermatology and Venereology, Lund University, Biomedical Center, Tornavägen 10, SE-22184 Lund, Sweden
b Department of Clinical Sciences, Section of Clinical and Experimental Infectious Medicine, Lund University, Biomedical Center, Tornavägen 10, SE-22184 Lund, Sweden
c Department of Pharmacy, Uppsala University, SE-751 23, Uppsala, Sweden
Abstract:Antimicrobial peptides are generated during activation of the complement system Nordahl et al. Proc. Natl. Acad. Sci. U. S. A. 2004, 101:16879-16884]. Here we show that the anaphylatoxin C3a exerts antimicrobial effects against the yeast Candida. Fluorescence microscopy and electron microscopy analysis demonstrated that C3a-derived peptides bound to the cell surface of Candida, and induced membrane perturbations and release of extracellular material. Various Candida isolates were found to induce complement degradation, leading to generation of C3a. Arginine residues were found to be critical for the antifungal and membrane breaking activity of a C3a-derived antimicrobial peptide, CNY21 (C3a; Cys57-Arg77). A CNY21 variant with increased positive net charge displayed enhanced antifungal activity. Thus, C3a-derived peptides can be utilized as templates in the development of peptide-based antifungal therapies.
Keywords:AMP  antimicrobial peptides  CF  carboxyfluorescein  cfu  colony-forming units  DOPA  1  2-Dioleoyl-sn-Glycero-3-Phosphate  monosodium salt  DOPC  1  2-dioleoyl-sn-Glycero-3-phosphocholine  Low-EEO  low-electroendosmotisistype agarose gel  MALDI-TOF  matrix-assisted laser desorption/ionization time-of-flight  MEC  minimal effective concentration  RDA  radial diffusion assay  TAMRA  Tetramethylrhodamine  YPD  yeast extract-peptone-dextrose
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