Literature DB >> 7768152

Potential therapeutic applications of magainins and other antimicrobial agents of animal origin.

L Jacob1, M Zasloff.   

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.

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Year:  1994        PMID: 7768152     DOI: 10.1002/9780470514658.ch12

Source DB:  PubMed          Journal:  Ciba Found Symp        ISSN: 0300-5208


  43 in total

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Review 2.  Antimicrobial peptides: current status and therapeutic potential.

Authors:  Andreas R Koczulla; Robert Bals
Journal:  Drugs       Date:  2003       Impact factor: 9.546

Review 3.  Nonmammalian vertebrate antibiotic peptides.

Authors:  P Síma; I Trebichavský; K Sigler
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Review 4.  Cationic antimicrobial peptides in clinical development, with special focus on thanatin and heliomicin.

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Review 5.  Applications of biological pores in nanomedicine, sensing, and nanoelectronics.

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6.  Characterization of the structure and membrane interaction of the antimicrobial peptides aurein 2.2 and 2.3 from Australian southern bell frogs.

Authors:  Yeang-Ling Pan; John T-J Cheng; John Hale; Jinhe Pan; Robert E W Hancock; Suzana K Straus
Journal:  Biophys J       Date:  2007-01-26       Impact factor: 4.033

Review 7.  Studies on anticancer activities of antimicrobial peptides.

Authors:  David W Hoskin; Ayyalusamy Ramamoorthy
Journal:  Biochim Biophys Acta       Date:  2007-11-22

Review 8.  On the physiology and pathophysiology of antimicrobial peptides.

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Journal:  Mol Med       Date:  2008-11-10       Impact factor: 6.354

9.  Importance of residue 13 and the C-terminus for the structure and activity of the antimicrobial peptide aurein 2.2.

Authors:  John T J Cheng; John D Hale; Jason Kindrachuk; Håvard Jenssen; Havard Jessen; Melissa Elliott; Robert E W Hancock; Suzana K Straus
Journal:  Biophys J       Date:  2010-11-03       Impact factor: 4.033

Review 10.  Pexiganan acetate.

Authors:  H M Lamb; L R Wiseman
Journal:  Drugs       Date:  1998-12       Impact factor: 9.546

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