Literature DB >> 10727928

Maculatin 1.1, an anti-microbial peptide from the Australian tree frog, Litoria genimaculata solution structure and biological activity.

B C Chia1, J A Carver, T D Mulhern, J H Bowie.   

Abstract

The dorsal glands of Australian tree frogs from the Litoria species contain a diversity of antibiotic peptides that forms part of the defence system of the animal. Here, the antibiotic activity and structure of maculatin 1.1, a 21 amino acid peptide from Litoria genimaculata, are compared. The activity data on maculatin 1.1 and a series of its analogues imply that the mechanism of action of maculatin 1.1 involves binding to, and subsequent lysis of, the bacterial cell membrane. The structure of maculatin 1.1 was determined using NMR spectroscopy in a trifluoroethanol/water mixture and when incorporated into dodecylphosphocholine micelles. Under both conditions, the peptide adopts a very similar conformation, i.e. a helical structure with a central kink in the vicinity of Pro15. The kink allows the peptide to adopt a well-defined amphipathic conformation along its entire length. The similar structures determined under both solvent conditions imply that structures of membrane-interacting peptides in trifluoroethanol/water mixtures are representative of those adopted in a membrane environment, e.g. when incorporated into micelles. The synthetic Ala15 analogue of maculatin 1.1 has markedly reduced activity and its NMR-derived structure is a well-defined helix, which lacks the central kink and flexibility of the parent molecule. It is concluded that the kink is important for full biological activity of the peptide, probably because it allows maximum amphipathicity of the peptide to facilitate interaction with the membrane. The structure of maculatin 1.1 is compared with a related peptide, caerin 1.1 [Wong, H., Bowie, J.H. and Carver, J.A. (1997) Eur. J. Biochem. 247, 545-557], which has an additional central proline residue and enhanced central flexibility compared with maculatin 1.1. The role of central flexibility within antibiotic peptides in their interaction with bacterial membranes is discussed.

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Year:  2000        PMID: 10727928     DOI: 10.1046/j.1432-1327.2000.01089.x

Source DB:  PubMed          Journal:  Eur J Biochem        ISSN: 0014-2956


  28 in total

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Review 2.  Nonmammalian vertebrate antibiotic peptides.

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4.  Population trends associated with skin peptide defenses against chytridiomycosis in Australian frogs.

Authors:  Douglas C Woodhams; Louise A Rollins-Smith; Cynthia Carey; Laura Reinert; Michael J Tyler; Ross A Alford
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5.  Direct visualization of membrane leakage induced by the antibiotic peptides: maculatin, citropin, and aurein.

Authors:  Ernesto E Ambroggio; Frances Separovic; John H Bowie; Gerardo D Fidelio; Luis A Bagatolli
Journal:  Biophys J       Date:  2005-07-01       Impact factor: 4.033

6.  Dye-release assay for investigation of antimicrobial peptide activity in a competitive lipid environment.

Authors:  Marc-Antoine Sani; Eve Gagne; John D Gehman; Thomas C Whitwell; Frances Separovic
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7.  NMR structure of a viral peptide inserted in artificial membranes: a view on the early steps of the birnavirus entry process.

Authors:  Marie Galloux; Sonia Libersou; Isabel D Alves; Rodrigue Marquant; Gilmar F Salgado; Human Rezaei; Jean Lepault; Bernard Delmas; Serge Bouaziz; Nelly Morellet
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8.  Bacteria May Cope Differently from Similar Membrane Damage Caused by the Australian Tree Frog Antimicrobial Peptide Maculatin 1.1.

Authors:  Marc-Antoine Sani; Sónia Troeira Henriques; Daniel Weber; Frances Separovic
Journal:  J Biol Chem       Date:  2015-06-22       Impact factor: 5.157

9.  Role of proline, cysteine and a disulphide bridge in the structure and activity of the anti-microbial peptide gaegurin 5.

Authors:  Sang-Ho Park; Hyung-Eun Kim; Chi-Man Kim; Hee-Jeong Yun; Eung-Chil Choi; Bong-Jin Lee
Journal:  Biochem J       Date:  2002-11-15       Impact factor: 3.857

10.  Maculatin 1.1 disrupts Staphylococcus aureus lipid membranes via a pore mechanism.

Authors:  M-A Sani; T C Whitwell; J D Gehman; R M Robins-Browne; N Pantarat; T J Attard; E C Reynolds; N M O'Brien-Simpson; F Separovic
Journal:  Antimicrob Agents Chemother       Date:  2013-05-20       Impact factor: 5.191

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