Literature DB >> 3427183

Incorporation kinetics in a membrane, studied with the pore-forming peptide alamethicin.

G Schwarz1, H Gerke, V Rizzo, S Stankowski.   

Abstract

The reaction of fluorescence-labeled alamethicin with unilamellar phospholipid vesicles (DOPC and DMPC) has been investigated in a stopped-flow apparatus. Clearly single exponential time functions have been observed at temperatures above the phase transition of the bilayer. This can be interpreted in terms of an essentially one-step incorporation process. The pseudo first-order forward rate is found to be quite fast, falling in a range somewhat below the diffusion controlled upper bound. The data are quantitatively very well described on the basis of a simple mechanism. This comprises diffusion of peptide into the bilayer accompanied by a more or less slower change of the secondary structure. Aggregation of the incorporated molecules at higher concentrations is indicated to be comparatively rapid.

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Year:  1987        PMID: 3427183      PMCID: PMC1330173          DOI: 10.1016/S0006-3495(87)83263-0

Source DB:  PubMed          Journal:  Biophys J        ISSN: 0006-3495            Impact factor:   4.033


  16 in total

1.  Basic kinetics of binding and incorporation with supramolecular aggregates.

Authors:  G Schwarz
Journal:  Biophys Chem       Date:  1987-05-09       Impact factor: 2.352

2.  Statistical analysis of alamethicin channels in black lipid membranes.

Authors:  G Boheim
Journal:  J Membr Biol       Date:  1974       Impact factor: 1.843

3.  Structural and dipolar properties of the voltage-dependent pore former alamethicin in octanol/dioxane.

Authors:  G Schwarz; P Savko
Journal:  Biophys J       Date:  1982-08       Impact factor: 4.033

4.  Dipole moment of alamethicin as related to voltage-dependent conductance in lipid bilayers.

Authors:  R Yantorno; S Takashima; P Mueller
Journal:  Biophys J       Date:  1982-05       Impact factor: 4.033

5.  Mass spectrometric determination of molecular formulas for membrane-modifying antibiotics.

Authors:  K L Rinehart; J C Cook; H Meng; K L Olson; R C Pandey
Journal:  Nature       Date:  1977-10-27       Impact factor: 49.962

6.  Calibration of stopped-flow spectrophotometers using a two-step disulfide exchange reaction.

Authors:  C Paul; K Kirschner; G Haenisch
Journal:  Anal Biochem       Date:  1980-01-15       Impact factor: 3.365

7.  Characterization of dimyristoylphosphatidylcholine vesicles and their dimensional changes through the phase transition: molecular control of membrane morphology.

Authors:  A Watts; D Marsh; P F Knowles
Journal:  Biochemistry       Date:  1978-05-02       Impact factor: 3.162

8.  [Structure of liquid-crystalline phases of different phospholipids, monoglycerides, sphingolipids in the absence or presence of water].

Authors:  F Reiss-Husson
Journal:  J Mol Biol       Date:  1967-05-14       Impact factor: 5.469

9.  Pore formation in lipid membranes by alamethicin.

Authors:  U P Fringeli; M Fringeli
Journal:  Proc Natl Acad Sci U S A       Date:  1979-08       Impact factor: 11.205

10.  Voltage-dependent conductance induced by alamethicin-phospholipid conjugates in lipid bilayers.

Authors:  R Latorre; C G Miller; S Quay
Journal:  Biophys J       Date:  1981-12       Impact factor: 4.033

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  22 in total

1.  Fluctuations and the rate-limiting step of peptide-induced membrane leakage.

Authors:  C Mazzuca; B Orioni; M Coletta; F Formaggio; C Toniolo; G Maulucci; M De Spirito; B Pispisa; M Venanzi; L Stella
Journal:  Biophys J       Date:  2010-09-22       Impact factor: 4.033

2.  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

3.  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

4.  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

5.  Transduction of membrane tension by the ion channel alamethicin.

Authors:  L R Opsahl; W W Webb
Journal:  Biophys J       Date:  1994-01       Impact factor: 4.033

6.  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

7.  A synthetic S6 segment derived from KvAP channel self-assembles, permeabilizes lipid vesicles, and exhibits ion channel activity in bilayer lipid membrane.

Authors:  Richa Verma; Chetan Malik; Sarfuddin Azmi; Saurabh Srivastava; Subhendu Ghosh; Jimut Kanti Ghosh
Journal:  J Biol Chem       Date:  2011-05-18       Impact factor: 5.157

8.  Androctonin, a hydrophilic disulphide-bridged non-haemolytic anti-microbial peptide: a plausible mode of action.

Authors:  C Hetru; L Letellier; Z Oren; J A Hoffmann; Y Shai
Journal:  Biochem J       Date:  2000-02-01       Impact factor: 3.857

9.  Interaction of tetanus toxin with lipid vesicles. Effects of pH, surface charge, and transmembrane potential on the kinetics of channel formation.

Authors:  G Menestrina; S Forti; F Gambale
Journal:  Biophys J       Date:  1989-03       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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