Literature DB >> 8086412

Spectrum of antimicrobial activity and assembly of dermaseptin-b and its precursor form in phospholipid membranes.

J Strahilevitz1, A Mor, P Nicolas, Y Shai.   

Abstract

Dermaseptins are 27-34 amino acid antimicrobial peptides that irreversibly inhibit growth of pathogenic filamentous fungi, in addition to their ability to inhibit the growth of bacteria, yeasts, and protozoa. Synthetic peptides, with sequences corresponding to dermaseptin-b (DS-b) and its N-terminal extended precursor form dermaseptin-B (DS-B), were synthesized and investigated with respect to their spectrum of antimicrobial activity and their mode of interaction with model membranes composed of PS or PC/PS phospholipids. We found that DS-B is much more potent than DS-b against all microorganisms tested. Furthermore, despite significant structural identity between DS-b and DS-S (Pouny et al., 1992), only the former is highly effective at inhibiting the growth of filamentous fungi. The peptides were labeled selectively at their N-terminal amino acid with either 7-nitrobenz-2-oxa-1,3-diazol-4-yl (NBD) or rhodamine fluorescent probes, which facilitated the determination of their partition coefficients with phospholipid membranes and their organization in their membrane-bound state. The partition coefficients of DS-B are 10-fold higher than those of DS-b and DS-S, with both acidic and zwitterionic phospholipid vesicles. This may explain the ability of DS-B to permeate both types of vesicles efficiently. Furthermore, while both DS-b and DS-B interact with phospholipid membranes in a noncooperative manner, they are self-associated in their membrane-bound state. This noncooperative binding probably prevents aggregation of the peptides on the surface of outer bacterial membranes, and assists them in efficiently diffusing into the inner target membranes. The exceptional property of DS-B to bind strongly to phospholipid membranes and to form small bundles correlates with its high potential to kill yeast and filamentous fungi. As a molecular model, dermaseptins may be of potential interest in drug design, particularly in antifungal warfare.

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Year:  1994        PMID: 8086412     DOI: 10.1021/bi00202a014

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  31 in total

1.  Antimalarial activities of dermaseptin S4 derivatives.

Authors:  M Krugliak; R Feder; V Y Zolotarev; L Gaidukov; A Dagan; H Ginsburg; A Mor
Journal:  Antimicrob Agents Chemother       Date:  2000-09       Impact factor: 5.191

2.  Thermodynamics of Micelle Formation and Membrane Fusion Modulate Antimicrobial Lipopeptide Activity.

Authors:  Dejun Lin; Alan Grossfield
Journal:  Biophys J       Date:  2015-08-18       Impact factor: 4.033

3.  Secondary structure, membrane localization, and coassembly within phospholipid membranes of synthetic segments derived from the N- and C-termini regions of the ROMK1 K+ channel.

Authors:  I Ben-Efraim; Y Shai
Journal:  Protein Sci       Date:  1996-11       Impact factor: 6.725

4.  Mechanism of membrane activity of the antibiotic trichogin GA IV: a two-state transition controlled by peptide concentration.

Authors:  Claudia Mazzuca; Lorenzo Stella; Mariano Venanzi; Fernando Formaggio; Claudio Toniolo; Basilio Pispisa
Journal:  Biophys J       Date:  2005-02-18       Impact factor: 4.033

5.  Role of peptide hydrophobicity in the mechanism of action of alpha-helical antimicrobial peptides.

Authors:  Yuxin Chen; Michael T Guarnieri; Adriana I Vasil; Michael L Vasil; Colin T Mant; Robert S Hodges
Journal:  Antimicrob Agents Chemother       Date:  2006-12-11       Impact factor: 5.191

Review 6.  Cell-penetrating peptides and antimicrobial peptides: how different are they?

Authors:  Sónia Troeira Henriques; Manuel Nuno Melo; Miguel A R B Castanho
Journal:  Biochem J       Date:  2006-10-01       Impact factor: 3.857

7.  Molecular dynamics investigation of the influence of anionic and zwitterionic interfaces on antimicrobial peptides' structure: implications for peptide toxicity and activity.

Authors:  Himanshu Khandelia; Yiannis N Kaznessis
Journal:  Peptides       Date:  2005-12-01       Impact factor: 3.750

8.  Immobilization of Escherichia coli cells by use of the antimicrobial peptide cecropin P1.

Authors:  Kalvin Gregory; Charlene M Mello
Journal:  Appl Environ Microbiol       Date:  2005-03       Impact factor: 4.792

9.  Production of a Recombinant Dermaseptin Peptide in Nicotiana tabacum Hairy Roots with Enhanced Antimicrobial Activity.

Authors:  Marzieh Varasteh Shams; Farhad Nazarian-Firouzabadi; Ahmad Ismaili; Reza Shirzadian-Khorramabad
Journal:  Mol Biotechnol       Date:  2019-04       Impact factor: 2.695

10.  Antimicrobial peptides and induced membrane curvature: geometry, coordination chemistry, and molecular engineering.

Authors:  Nathan W Schmidt; Gerard C L Wong
Journal:  Curr Opin Solid State Mater Sci       Date:  2013-08       Impact factor: 11.354

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