Antifungal activity of C3a and C3a-derived peptides against Candida.
(2007) In Biochimica et Biophysica Acta - Biomembranes 1768(2). p.346-353- Abstract
- Antimicrobial peptides are generated during activation of the complement system [Nordahl et al. Proc. Nat1. 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; Cys(57)-Arg(77)). A CNY21 variant with... (More)
- Antimicrobial peptides are generated during activation of the complement system [Nordahl et al. Proc. Nat1. 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; Cys(57)-Arg(77)). 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. (c) 2006 Elsevier B.V All rights reserved. (Less)
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/163998
- author
- Sonesson, Andreas LU ; Ringstad, Lovisa ; Nordahl, Emma LU ; Malmsten, Martin LU ; Mörgelin, Matthias LU and Schmidtchen, Artur LU
- organization
- publishing date
- 2007
- type
- Contribution to journal
- publication status
- published
- subject
- keywords
- atopic dermatitis, Candida, innate immunity, antimicrobial peptides, complement, structure-activity relationship study
- in
- Biochimica et Biophysica Acta - Biomembranes
- volume
- 1768
- issue
- 2
- pages
- 346 - 353
- publisher
- Elsevier
- external identifiers
-
- wos:000244384600017
- scopus:33846378792
- pmid:17169328
- ISSN
- 0005-2736
- DOI
- 10.1016/j.bbamem.2006.10.017
- language
- English
- LU publication?
- yes
- id
- ebdd70c8-6c3c-4515-93e6-1452aecbadf6 (old id 163998)
- alternative location
- http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=17169328&dopt=Abstract
- date added to LUP
- 2016-04-01 15:52:49
- date last changed
- 2022-03-30 03:41:15
@article{ebdd70c8-6c3c-4515-93e6-1452aecbadf6, abstract = {{Antimicrobial peptides are generated during activation of the complement system [Nordahl et al. Proc. Nat1. 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; Cys(57)-Arg(77)). 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. (c) 2006 Elsevier B.V All rights reserved.}}, author = {{Sonesson, Andreas and Ringstad, Lovisa and Nordahl, Emma and Malmsten, Martin and Mörgelin, Matthias and Schmidtchen, Artur}}, issn = {{0005-2736}}, keywords = {{atopic dermatitis; Candida; innate immunity; antimicrobial peptides; complement; structure-activity relationship study}}, language = {{eng}}, number = {{2}}, pages = {{346--353}}, publisher = {{Elsevier}}, series = {{Biochimica et Biophysica Acta - Biomembranes}}, title = {{Antifungal activity of C3a and C3a-derived peptides against Candida.}}, url = {{http://dx.doi.org/10.1016/j.bbamem.2006.10.017}}, doi = {{10.1016/j.bbamem.2006.10.017}}, volume = {{1768}}, year = {{2007}}, }