Literature DB >> 12770873

The role of the dielectric barrier in narrow biological channels: a novel composite approach to modeling single-channel currents.

Artem B Mamonov1, Rob D Coalson, Abraham Nitzan, Maria G Kurnikova.   

Abstract

A composite continuum theory for calculating ion current through a protein channel of known structure is proposed, which incorporates information about the channel dynamics. The approach is utilized to predict current through the Gramicidin A ion channel, a narrow pore in which the applicability of conventional continuum theories is questionable. The proposed approach utilizes a modified version of Poisson-Nernst-Planck (PNP) theory, termed Potential-of-Mean-Force-Poisson-Nernst-Planck theory (PMFPNP), to compute ion currents. As in standard PNP, ion permeation is modeled as a continuum drift-diffusion process in a self-consistent electrostatic potential. In PMFPNP, however, information about the dynamic relaxation of the protein and the surrounding medium is incorporated into the model of ion permeation by including the free energy of inserting a single ion into the channel, i.e., the potential of mean force along the permeation pathway. In this way the dynamic flexibility of the channel environment is approximately accounted for. The PMF profile of the ion along the Gramicidin A channel is obtained by combining an equilibrium molecular dynamics (MD) simulation that samples dynamic protein configurations when an ion resides at a particular location in the channel with a continuum electrostatics calculation of the free energy. The diffusion coefficient of a potassium ion within the channel is also calculated using the MD trajectory. Therefore, except for a reasonable choice of dielectric constants, no direct fitting parameters enter into this model. The results of our study reveal that the channel response to the permeating ion produces significant electrostatic stabilization of the ion inside the channel. The dielectric self-energy of the ion remains essentially unchanged in the course of the MD simulation, indicating that no substantial changes in the protein geometry occur as the ion passes through it. Also, the model accounts for the experimentally observed saturation of ion current with increase of the electrolyte concentration, in contrast to the predictions of standard PNP theory.

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Year:  2003        PMID: 12770873      PMCID: PMC1302949          DOI: 10.1016/S0006-3495(03)75095-4

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


  44 in total

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Journal:  Proteins       Date:  1986-09
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  31 in total

1.  Anion pathway and potential energy profiles along curvilinear bacterial ClC Cl- pores: electrostatic effects of charged residues.

Authors:  Gennady V Miloshevsky; Peter C Jordan
Journal:  Biophys J       Date:  2004-02       Impact factor: 4.033

2.  Ionic permeation free energy in gramicidin: a semimicroscopic perspective.

Authors:  Vladimir L Dorman; Peter C Jordan
Journal:  Biophys J       Date:  2004-06       Impact factor: 4.033

3.  Quantum dynamics in continuum for proton transport--generalized correlation.

Authors:  Duan Chen; Guo-Wei Wei
Journal:  J Chem Phys       Date:  2012-04-07       Impact factor: 3.488

4.  Energy variational analysis of ions in water and channels: Field theory for primitive models of complex ionic fluids.

Authors:  Bob Eisenberg; Yunkyong Hyon; Chun Liu
Journal:  J Chem Phys       Date:  2010-09-14       Impact factor: 3.488

Review 5.  The new nanophysiology: regulation of ionic flow in neuronal subcompartments.

Authors:  David Holcman; Rafael Yuste
Journal:  Nat Rev Neurosci       Date:  2015-10-14       Impact factor: 34.870

6.  Influence of protein flexibility on the electrostatic energy landscape in gramicidin A.

Authors:  Ben Corry; Shin-Ho Chung
Journal:  Eur Biophys J       Date:  2004-11-05       Impact factor: 1.733

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Authors:  Marcel Aguilella-Arzo; Vicente M Aguilella; R S Eisenberg
Journal:  Eur Biophys J       Date:  2005-03-09       Impact factor: 1.733

8.  Theoretical studies of the M2 transmembrane segment of the glycine receptor: models of the open pore structure and current-voltage characteristics.

Authors:  Mary Hongying Cheng; Michael Cascio; Rob D Coalson
Journal:  Biophys J       Date:  2005-06-10       Impact factor: 4.033

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Authors:  Toby W Allen; Olaf S Andersen; Benoit Roux
Journal:  Biophys J       Date:  2006-02-24       Impact factor: 4.033

10.  On the importance of atomic fluctuations, protein flexibility, and solvent in ion permeation.

Authors:  Toby W Allen; O S Andersen; Benoit Roux
Journal:  J Gen Physiol       Date:  2004-12       Impact factor: 4.086

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