Literature DB >> 3606990

Alamethicin incorporation in lipid bilayers: a thermodynamic study.

V Rizzo, S Stankowski, G Schwarz.   

Abstract

Interaction of the peptide antibiotic alamethicin with phospholipid vesicles has been monitored by changes in its circular dichroic and fluorescent properties. The data are consistent with an incorporation of the peptide in the lipid bilayer. Aggregation of alamethicin in the membrane phase is evident from a characteristic concentration dependence of the incorporation, reflecting the existence of a critical concentration. The data can be fully understood in terms of a theoretical approach that includes aggregation and thermodynamic nonideality. Thermodynamic parameters of the peptide-lipid interaction have been evaluated under a variety of conditions of temperature, ionic strength, and lipid type (saturated and unsaturated fatty acid chains). From the results obtained in this study, one can extrapolate to the incorporation behavior of alamethicin at low concentrations, as they are typical for measurements of conductance across planar lipid films. This leads to a simple explanation of the voltage-gating mechanism of alamethicin in a straightforward way.

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Year:  1987        PMID: 3606990     DOI: 10.1021/bi00384a015

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


  28 in total

1.  Membrane partitioning of the cleavage peptide in flock house virus.

Authors:  D T Bong; A Janshoff; C Steinem; M R Ghadiri
Journal:  Biophys J       Date:  2000-02       Impact factor: 4.033

2.  The properties of ion channels formed by zervamicins.

Authors:  P Balaram; K Krishna; M Sukumar; I R Mellor; M S Sansom
Journal:  Eur Biophys J       Date:  1992       Impact factor: 1.733

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.  Dynamics and aggregation of the peptide ion channel alamethicin. Measurements using spin-labeled peptides.

Authors:  S J Archer; J F Ellena; D S Cafiso
Journal:  Biophys J       Date:  1991-08       Impact factor: 4.033

5.  Voltage-dependent conductance for alamethicin in phospholipid vesicles. A test for the mechanism of gating.

Authors:  S J Archer; D S Cafiso
Journal:  Biophys J       Date:  1991-08       Impact factor: 4.033

6.  Pore formation kinetics in membranes, determined from the release of marker molecules out of liposomes or cells.

Authors:  G Schwarz; C H Robert
Journal:  Biophys J       Date:  1990-09       Impact factor: 4.033

7.  The structure and organization within the membrane of the helices composing the pore-forming domain of Bacillus thuringiensis delta-endotoxin are consistent with an "umbrella-like" structure of the pore.

Authors:  E Gazit; P La Rocca; M S Sansom; Y Shai
Journal:  Proc Natl Acad Sci U S A       Date:  1998-10-13       Impact factor: 11.205

8.  Structural features that modulate the transmembrane migration of a hydrophobic peptide in lipid vesicles.

Authors:  S Jayasinghe; M Barranger-Mathys; J F Ellena; C Franklin; D S Cafiso
Journal:  Biophys J       Date:  1998-06       Impact factor: 4.033

9.  Effect of protein aggregation in the aqueous phase on the binding of membrane proteins to membranes.

Authors:  R Doebler; N Başaran; H Goldston; P W Holloway
Journal:  Biophys J       Date:  1999-02       Impact factor: 4.033

10.  Alamethicin and related peptaibols--model ion channels.

Authors:  M S Sansom
Journal:  Eur Biophys J       Date:  1993       Impact factor: 1.733

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