Literature DB >> 2454676

Evaluation of surface tension and ion occupancy effects on gramicidin A channel lifetime.

A Ring1, J Sandblom.   

Abstract

The surface tension of glycerylmonooleate-hexadecane lipid bilayer membranes and the lifetime of gramicidin A channels were measured at various concentrations of the surrounding solutions. For HCl the surface tension is essentially constant at approximately 5 mN/m up to approximately 1 M, whereas the average lifetime increases approximately 40-fold. At higher concentrations the surface tension decreases markedly. For CsCl the surface tension is constant up to about 1 M then increases with salt level. The average lifetime in this case increases about sixfold. In both cases the lifetime levels off and even decreases at higher salt levels. The increase in lifetime observed with ion activity is therefore qualitatively different from, and not explained by, the established dependence of lifetime on membrane properties (Elliot, J.R., D. Needham, J.P. Dilger, and D.A. Haydon. 1983. Biochim. Biophys. Acta. 735:95-103). We have previously proposed that ion occupancy is a determinant of channel stability, and to test this hypothesis the voltage dependence of channel lifetime was measured in asymmetrical solutions. For the case of a potassium chloride solution on one side of the membrane and a hydrogen chloride solution, on the other, the voltage dependence of the lifetime is asymmetrical. The asymmetry is such that when the electrical field is applied in the direction of the chemical gradient for each of the ions, the channel lifetime approaches, at increasing field strengths, that of a symmetrical solution of the respective ion. The voltage dependence of the surface tension, on the other hand, is negligible for the range of voltages used. These results, and the earlier findings that the order of the lifetimes for the alkali cations generally agree with the order of the permeability selectivity of the gramicidin A channel, support the hypothesis that ion occupancy is a major factor determining the lifetime of gramicidin A channels. The effects of multivalent blockers and osmotic agents were also tested. Ba2", La3+,and Mg2" decrease the lifetime and conductance markedly. Sucrose and urea increase the lifetime and decrease the conductance. The voltage dependence of the lifetime in symmetrical solutions was examined. Contrary to previous reports it was found that the lifetimes for K+, Cs', and H+ are voltage dependent. For 0.5 M HCI the lifetime decreases monotonically by .60% at 150 mV, and for 0.5 M KCI the lifetime increases by -60% at 200 mV. Below 10 mM there is no effect of voltage for H+, K+, and Cs+. These effects of blockers, osmotic agents, and voltage on the lifetime, as well as the lack of effect of voltage at low salt levels, are consistent with the occupancy hypothesis.

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Year:  1988        PMID: 2454676      PMCID: PMC1330228          DOI: 10.1016/S0006-3495(88)83134-5

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


  27 in total

1.  Brief closures of gramicidin A channels in lipid bilayer membranes.

Authors:  A Ring
Journal:  Biochim Biophys Acta       Date:  1986-04-25

2.  Conformation of the gramicidin A transmembrane channel: A 13C nuclear magnetic resonance study of 13C-enriched gramicidin in phosphatidylcholine vesicles.

Authors:  S Weinstein; B A Wallace; J S Morrow; W R Veatch
Journal:  J Mol Biol       Date:  1980-10-15       Impact factor: 5.469

3.  Structure and dynamics of ion transport through gramicidin A.

Authors:  D H Mackay; P H Berens; K R Wilson; A T Hagler
Journal:  Biophys J       Date:  1984-08       Impact factor: 4.033

4.  Gramicidin forms multi-state rectifying channels.

Authors:  D Busath; G Szabo
Journal:  Nature       Date:  1981-11-26       Impact factor: 49.962

5.  Molecular dynamics study of ion transport in transmembrane protein channels.

Authors:  W Fischer; J Brickmann; P Läuger
Journal:  Biophys Chem       Date:  1981-04       Impact factor: 2.352

6.  Ionic selectivity, saturation, and block in gramicidin A channels. II. Saturation behavior of single channel conductances and evidence for the existence of multiple binding sites in the channel.

Authors:  E Neher; J Sandblom; G Eisenman
Journal:  J Membr Biol       Date:  1978-04-26       Impact factor: 1.843

7.  The dependence of the conductance and lifetime of gramicidin channels on the thickness and tension of lipid bilayers.

Authors:  V S Rudnev; L N Ermishkin; L A Fonina
Journal:  Biochim Biophys Acta       Date:  1981-03-20

8.  Rate theory calculation of gramicidin single-channel currents using NMR-derived rate constants.

Authors:  D W Urry; C M Venkatachalam; A Spisni; P Läuger; M A Khaled
Journal:  Proc Natl Acad Sci U S A       Date:  1980-04       Impact factor: 11.205

9.  Influence of membrane thickness and ion concentration on the properties of the gramicidin a channel. Autocorrelation, spectral power density, relaxation and single-channel studies.

Authors:  H A Kolb; E Bamberg
Journal:  Biochim Biophys Acta       Date:  1977-01-04

10.  Is the gramicidin a transmembrane channel single-stranded or double-stranded helix? A simple unequivocal determination.

Authors:  D W Urry; T L Trapane; K U Prasad
Journal:  Science       Date:  1983-09-09       Impact factor: 47.728

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  7 in total

1.  Voltage-dependent formation of gramicidin channels in lipid bilayers.

Authors:  J Sandblom; J Galvanovskis; B Jilderos
Journal:  Biophys J       Date:  2001-08       Impact factor: 4.033

2.  Monitoring the surface tension of lipid membranes by a bubble method.

Authors:  A Ring
Journal:  Pflugers Arch       Date:  1992-03       Impact factor: 3.657

3.  Cation-Selective Channel Regulated by Anions According to Their Hofmeister Ranking.

Authors:  Philip A Gurnev; Torri C Roark; Horia I Petrache; Alexander J Sodt; Sergey M Bezrukov
Journal:  Angew Chem Int Ed Engl       Date:  2017-02-15       Impact factor: 15.336

4.  Modulation of gramicidin A open channel lifetime by ion occupancy.

Authors:  A Ring; J Sandblom
Journal:  Biophys J       Date:  1988-04       Impact factor: 4.033

5.  On the origin of closing flickers in gramicidin channels: a new hypothesis.

Authors:  Kathryn M Armstrong; Samuel Cukierman
Journal:  Biophys J       Date:  2002-03       Impact factor: 4.033

6.  Influence of ion occupancy and membrane deformation on gramicidin A channel stability in lipid membranes.

Authors:  A Ring
Journal:  Biophys J       Date:  1992-05       Impact factor: 4.033

Review 7.  Model ion channels: gramicidin and alamethicin.

Authors:  G A Woolley; B A Wallace
Journal:  J Membr Biol       Date:  1992-08       Impact factor: 1.843

  7 in total

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