Literature DB >> 9826603

Attenuation of proton currents by methanol in a dioxolane-linked gramicidin A channel in different lipid bilayers.

E P Quigley1, A J Emerick, D S Crumrine, S Cukierman.   

Abstract

The mobility of protons in a dioxolane-linked gramicidin A channel (D1) is comparable to the mobility of protons in aqueous solutions (Cukierman, S., E. P. Quigley, and D. S. Crumrine. 1997. Biophys. J. 73:2489-2502). Aliphatic alcohols decrease the mobility of H+ in aqueous solutions. In this study, the effects of methanol on proton conduction through D1 channels were investigated in different lipid bilayers and at different HCl concentrations. Methanol attenuated H+ currents in a voltage-independent manner. Attenuation of proton currents was also independent of H+ concentrations in solution. In phospholipid bilayers, methanol decreased the single channel conductance to protons without affecting the binding affinity of protons to bilayers. In glycerylmonooleate membranes, the attenuation of single channel proton conductances qualitatively resembled the decrease of conductivities of HCl solutions by methanol. However, in both types of lipid bilayers, single channel proton conductances through D1 channels were considerably more attenuated than the conductivities of different HCl solutions. This suggests that methanol modulates single proton currents through D1 channels. It is proposed that, on average, one methanol molecule binds to a D1 channel, and attenuates H+ conductance. The Gibbs free energy of this process (DeltaG0) is approximately 1.2 kcal/mol, which is comparable to the free energy of decrease of HCl conductivity in methanol solutions (1.6 kcal/mol). Apolar substances like urea and glucose that do not transport protons in HCl solutions and do not permeate D1 channels decreased solution conductivity and single channel conductance by a considerably larger proportion than methanol. Cs+ currents through D1 channels were considerably less (fivefold) attenuated by methanol than proton currents. It is proposed that methanol partitions inside the pore of gramicidin channels and delays the transfer of protons between water and methanol molecules, causing a significant attenuation of the single channel proton conductance. Gramicidin channels offer an interesting experimental model to study proton hopping along a single chain of water molecules interrupted by a single methanol molecule.

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Year:  1998        PMID: 9826603      PMCID: PMC1299954          DOI: 10.1016/S0006-3495(98)77724-0

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


  21 in total

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Journal:  Methods Enzymol       Date:  1986       Impact factor: 1.600

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Journal:  Proc Natl Acad Sci U S A       Date:  1971-08       Impact factor: 11.205

3.  The gramicidin A transmembrane channel: a proposed pi(L,D) helix.

Authors:  D W Urry
Journal:  Proc Natl Acad Sci U S A       Date:  1971-03       Impact factor: 11.205

4.  The gramicidin A channel: a review of its permeability characteristics with special reference to the single-file aspect of transport.

Authors:  A Finkelstein; O S Andersen
Journal:  J Membr Biol       Date:  1981-04-30       Impact factor: 1.843

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Authors:  O S Andersen
Journal:  Biophys J       Date:  1983-02       Impact factor: 4.033

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Journal:  Biochim Biophys Acta       Date:  1977-03-17

Review 7.  Hydrogen bonded chain mechanisms for proton conduction and proton pumping.

Authors:  J F Nagle; S Tristram-Nagle
Journal:  J Membr Biol       Date:  1983       Impact factor: 1.843

8.  Number of water molecules coupled to the transport of sodium, potassium and hydrogen ions via gramicidin, nonactin or valinomycin.

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Journal:  Biochim Biophys Acta       Date:  1978-09-22

9.  Access resistance of a small circular pore.

Authors:  J E Hall
Journal:  J Gen Physiol       Date:  1975-10       Impact factor: 4.086

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Authors:  P A Rosenberg; A Finkelstein
Journal:  J Gen Physiol       Date:  1978-09       Impact factor: 4.086

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  7 in total

1.  Covalently linked gramicidin channels: effects of linker hydrophobicity and alkaline metals on different stereoisomers.

Authors:  K M Armstrong; E P Quigley; P Quigley; D S Crumrine; S Cukierman
Journal:  Biophys J       Date:  2001-04       Impact factor: 4.033

2.  Proton mobilities in water and in different stereoisomers of covalently linked gramicidin A channels.

Authors:  S Cukierman
Journal:  Biophys J       Date:  2000-04       Impact factor: 4.033

3.  The conduction of protons in different stereoisomers of dioxolane-linked gramicidin A channels.

Authors:  E P Quigley; P Quigley; D S Crumrine; S Cukierman
Journal:  Biophys J       Date:  1999-11       Impact factor: 4.033

4.  Modulation of proton transfer in the water wire of dioxolane-linked gramicidin channels by lipid membranes.

Authors:  C M de Godoy; S Cukierman
Journal:  Biophys J       Date:  2001-09       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.  Proton transfer in gramicidin water wires in phospholipid bilayers: attenuation by phosphoethanolamine.

Authors:  Anatoly Chernyshev; Samuel Cukierman
Journal:  Biophys J       Date:  2006-04-14       Impact factor: 4.033

7.  Proton transfer in water wires in proteins: modulation by local constraint and polarity in gramicidin a channels.

Authors:  Shasikala Narayan; Debra L Wyatt; David S Crumrine; Samuel Cukierman
Journal:  Biophys J       Date:  2007-05-11       Impact factor: 4.033

  7 in total

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