Abstract

The voltage-dependent anion channel (VDAC) forms the major pore in the outer mitochondrial membrane. Its high conducting open state features a moderate anion selectivity. There is some evidence indicating that the electrophysiological properties of VDAC vary with the salt concentration. Using a theoretical approach the molecular basis for this concentration dependence was investigated. Molecular dynamics simulations and continuum electrostatic calculations performed on the mouse VDAC1 isoform clearly demonstrate that the distribution of fixed charges in the channel creates an electric field, which determines the anion preference of VDAC at low salt concentration. Increasing the salt concentration in the bulk results in a higher concentration of ions in the VDAC wide pore. This event induces a large electrostatic screening of the charged residues promoting a less anion selective channel. Residues that are responsible for the electrostatic pattern of the channel were identified using the molecular dynamics trajectories. Some of these residues are found to be conserved suggesting that ion permeation between different VDAC species occurs through a common mechanism. This inference is buttressed by electrophysiological experiments performed on bean VDAC32 protein akin to mouse VDAC.

Highlights

  • The voltage-dependent anion channel (VDAC) is the most abundant integral membrane protein of the mitochondrial outer membrane

  • At voltages close to 0 mV, the channel exists in a fully open state characterized by a high conductance of about 4 nS [7,8], which is compatible with the magnitude of the metabolites flow into and out of the mitochondria

  • At the atomic detail, the ion translocation process at different salt concentrations using a combination of molecular dynamics (MD) and continuum electrostatic approaches carried out on the crystal structure of mVDAC1

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Summary

Introduction

The voltage-dependent anion channel (VDAC) is the most abundant integral membrane protein of the mitochondrial outer membrane. It is a key regulator of metabolite flow notably of adenosine nucleotides, sugars and inorganic ions and forms the main interface between the mitochondrial and the cytoplasmic metabolism [1]. Upon higher voltages (.620 mV) VDAC switches to partially closed states showing lower conductances for small ions and being no longer permeable to metabolites. This channel possesses a slight preference for inorganic anions over cations while it shows a reversed selectivity in most of its closed states [1,7,8,11]. There is some evidence that the electrophysiological properties (conductance, reversal potential) vary with the bulk salt concentration [7,8,9,12,13,14,15,16]

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