Literature DB >> 8994596

Permeation through an open channel: Poisson-Nernst-Planck theory of a synthetic ionic channel.

D Chen1, J Lear, B Eisenberg.   

Abstract

The synthetic channel [acetyl-(LeuSerSerLeuLeuSerLeu)3-CONH2]6 (pore diameter approximately 8 A, length approximately 30 A) is a bundle of six alpha-helices with blocked termini. This simple channel has complex properties, which are difficult to explain, even qualitatively, by traditional theories: its single-channel currents rectify in symmetrical solutions and its selectivity (defined by reversal potential) is a sensitive function of bathing solution. These complex properties can be fit quantitatively if the channel has fixed charge at its ends, forming a kind of macrodipole, bracketing a central charged region, and the shielding of the fixed charges is described by the Poisson-Nernst-Planck (PNP) equations. PNP fits current voltage relations measured in 15 solutions with an r.m.s. error of 3.6% using four adjustable parameters: the diffusion coefficients in the channel's pore DK = 2.1 x 10(-6) and DCl = 2.6 x 10(-7) cm2/s; and the fixed charge at the ends of the channel of +/- 0.12e (with unequal densities 0.71 M = 0.021e/A on the N-side and -1.9 M = -0.058e/A on the C-side). The fixed charge in the central region is 0.31e (with density P2 = 0.47 M = 0.014e/A). In contrast to traditional theories, PNP computes the electric field in the open channel from all of the charges in the system, by a rapid and accurate numerical procedure. In essence, PNP is a theory of the shielding of fixed (i.e., permanent) charge of the channel by mobile charge and by the ionic atmosphere in and near the channel's pore. The theory fits a wide range of data because the ionic contents and potential profile in the channel change significantly with experimental conditions, as they must, if the channel simultaneously satisfies the Poisson and Nernst-Planck equations and boundary conditions. Qualitatively speaking, the theory shows that small changes in the ionic atmosphere of the channel (i.e., shielding) make big changes in the potential profile and even bigger changes in flux, because potential is a sensitive function of charge and shielding, and flux is an exponential function of potential.

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Year:  1997        PMID: 8994596      PMCID: PMC1184300          DOI: 10.1016/S0006-3495(97)78650-8

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


  36 in total

1.  Constant fields and constant gradients in open ionic channels.

Authors:  D P Chen; V Barcilon; R S Eisenberg
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Journal:  Annu Rev Biophys Biophys Chem       Date:  1989

3.  Parameter estimation by least-squares methods.

Authors:  M L Johnson; L M Faunt
Journal:  Methods Enzymol       Date:  1992       Impact factor: 1.600

Review 4.  Channels as enzymes.

Authors:  R S Eisenberg
Journal:  J Membr Biol       Date:  1990-04       Impact factor: 1.843

Review 5.  Surface charges and ion channel function.

Authors:  W N Green; O S Andersen
Journal:  Annu Rev Physiol       Date:  1991       Impact factor: 19.318

Review 6.  Surmounting barriers in ionic channels.

Authors:  K E Cooper; P Y Gates; R S Eisenberg
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7.  Stochastic theory of singly occupied ion channels. II. Effects of access resistance and potential gradients extending into the bath.

Authors:  S W Chiu; E Jakobsson
Journal:  Biophys J       Date:  1989-01       Impact factor: 4.033

Review 8.  Diffusion theory and discrete rate constants in ion permeation.

Authors:  K E Cooper; P Y Gates; R S Eisenberg
Journal:  J Membr Biol       Date:  1988-12       Impact factor: 1.843

Review 9.  Ionic selectivity revisited: the role of kinetic and equilibrium processes in ion permeation through channels.

Authors:  G Eisenman; R Horn
Journal:  J Membr Biol       Date:  1983       Impact factor: 1.843

10.  Synthetic amphiphilic peptide models for protein ion channels.

Authors:  J D Lear; Z R Wasserman; W F DeGrado
Journal:  Science       Date:  1988-05-27       Impact factor: 47.728

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  47 in total

1.  Statistical mechanical equilibrium theory of selective ion channels.

Authors:  B Roux
Journal:  Biophys J       Date:  1999-07       Impact factor: 4.033

2.  Framework model for single proton conduction through gramicidin.

Authors:  M F Schumaker; R Pomès; B Roux
Journal:  Biophys J       Date:  2001-01       Impact factor: 4.033

3.  Tests of continuum theories as models of ion channels. II. Poisson-Nernst-Planck theory versus brownian dynamics.

Authors:  B Corry; S Kuyucak; S H Chung
Journal:  Biophys J       Date:  2000-05       Impact factor: 4.033

4.  Side-chain ionization states in a potassium channel.

Authors:  K M Ranatunga; I H Shrivastava; G R Smith; M S Sansom
Journal:  Biophys J       Date:  2001-03       Impact factor: 4.033

5.  Model channel ion currents in NaCl-extended simple point charge water solution with applied-field molecular dynamics.

Authors:  P S Crozier; D Henderson; R L Rowley; D D Busath
Journal:  Biophys J       Date:  2001-12       Impact factor: 4.033

6.  Properties of gap junction channels formed by Cx46 alone and in combination with Cx50.

Authors:  M G Hopperstad; M Srinivas; D C Spray
Journal:  Biophys J       Date:  2000-10       Impact factor: 4.033

7.  Electrostatic influence on ion transport through the alphaHL channel.

Authors:  M Misakian; J J Kasianowicz
Journal:  J Membr Biol       Date:  2003-10-01       Impact factor: 1.843

Review 8.  Gap junction channel gating.

Authors:  Feliksas F Bukauskas; Vytas K Verselis
Journal:  Biochim Biophys Acta       Date:  2004-03-23

9.  Selectivity and permeation in calcium release channel of cardiac muscle: alkali metal ions.

Authors:  D P Chen; L Xu; A Tripathy; G Meissner; B Eisenberg
Journal:  Biophys J       Date:  1999-03       Impact factor: 4.033

10.  Electrostatics and the ion selectivity of ligand-gated channels.

Authors:  C Adcock; G R Smith; M S Sansom
Journal:  Biophys J       Date:  1998-09       Impact factor: 4.033

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