Potential therapeutic applications of magainins and other antimicrobial agents of animal origin
- PMID: 7768152
- DOI: 10.1002/9780470514658.ch12
Potential therapeutic applications of magainins and other antimicrobial agents of animal origin
Abstract
Magainins are a family of linear, amphipathic, cationic antimicrobial peptides, 21 to 27 residues in length, found in the skin of Xenopus laevis. They kill microbial targets through disruption of membrane permeability. They exhibit selectivity, on the basis of their affinity for membranes which contain accessible acidic phospholipids, a property characterizing the cytoplasmic membranes of many species of bacteria. Magainins are broad-spectrum antimicrobial agents exhibiting cidal activity against Gram-negative and Gram-positive bacteria, fungi and protozoa. In addition these peptides lyse many types of murine and human cancer cells at concentrations 5-10-fold lower than normal human cells. Because of their selectivity, broad spectrum, low degree of bacterial resistance and ease of chemical synthesis, magainins are being developed as human therapeutic agents. The most advanced candidate is MSI-78, a 22-residue magainin analogue. This peptide is currently in human Phase IIb/III clinical trials in studies intended to evaluate its efficacy as a topical agent for the treatment of impetigo. Preclinical studies have demonstrated that analogues of magainin exhibit activity in vivo against malignant melanoma and ovarian cancer cells in mouse models. Intravenous administration of several magainin analogues has been shown to treat effectively systemic Escherichia coli infections in the mouse.
Similar articles
-
Antimicrobial properties of peptides from Xenopus granular gland secretions.FEBS Lett. 1988 Feb 15;228(2):337-40. doi: 10.1016/0014-5793(88)80027-9. FEBS Lett. 1988. PMID: 3125066
-
Interactions of an antimicrobial peptide, magainin 2, with outer and inner membranes of Gram-negative bacteria.Biochim Biophys Acta. 1997 Jul 5;1327(1):119-30. doi: 10.1016/s0005-2736(97)00051-5. Biochim Biophys Acta. 1997. PMID: 9247173
-
The Magainins: sequence factors relevant to increased antimicrobial activity and decreased hemolytic activity.Pept Res. 1988 Nov-Dec;1(2):81-6. Pept Res. 1988. PMID: 2980783
-
Magainins as paradigm for the mode of action of pore forming polypeptides.Biochim Biophys Acta. 1998 Nov 10;1376(3):391-400. doi: 10.1016/s0304-4157(98)00014-8. Biochim Biophys Acta. 1998. PMID: 9804997 Review.
-
Structure-activity studies on magainins and other host defense peptides.Biopolymers. 1995;37(2):105-22. doi: 10.1002/bip.360370206. Biopolymers. 1995. PMID: 7893944 Review.
Cited by
-
Peptide pheromone plantaricin a produced by Lactobacillus plantarum permeabilizes liver and kidney cells.J Membr Biol. 2010 Jun;235(2):121-9. doi: 10.1007/s00232-010-9263-4. Epub 2010 May 29. J Membr Biol. 2010. PMID: 20512319
-
Expression of an antimicrobial peptide via the chloroplast genome to control phytopathogenic bacteria and fungi.Plant Physiol. 2001 Nov;127(3):852-62. Plant Physiol. 2001. PMID: 11706168 Free PMC article.
-
ECAM is waiting for eCAM.Evid Based Complement Alternat Med. 2005 Dec;2(4):427-8. doi: 10.1093/ecam/neh135. Evid Based Complement Alternat Med. 2005. PMID: 16322798 Free PMC article. No abstract available.
-
Oxidation of the N-terminal gly-residue of peptides: stress study of pexiganan acetate in a drug formulation.Pharm Res. 2000 Feb;17(2):197-204. doi: 10.1023/a:1007521515109. Pharm Res. 2000. PMID: 10751035
-
Activity of the de novo engineered antimicrobial peptide WLBU2 against Pseudomonas aeruginosa in human serum and whole blood: implications for systemic applications.Antimicrob Agents Chemother. 2005 Aug;49(8):3208-16. doi: 10.1128/AAC.49.8.3208-3216.2005. Antimicrob Agents Chemother. 2005. PMID: 16048927 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Other Literature Sources
Medical