ABSTRACT
An explanation for the ionic selectivity of the bacterial potassium channel K(CS)A is offered, which is based on a comparison of energy interactions of lithium, sodium, and potassium cations with the atoms of the selective filter of an protein pore. Using quantum-chemical calculations, the presence of a deeper potential hole for potassium ions was discovered, which explains the energy preferableness in their permeability. It has been shown that the traditional methods of force field AMBER, CHARMM, OPLS in reference parametrization and also at their partial reparametrization give incorrect ratings of energy distribution of ions in the channel.
Subject(s)
Bacterial Proteins/chemistry , Models, Chemical , Potassium Channels/chemistry , Protein Structure, Quaternary , ThermodynamicsABSTRACT
A model study of the motion of Na+ ions in the cavity of membrane gramicidin channels was performed by the methods of quantum mechanics. An approximation of the distribution of the electrostatic potential along the channel axis, determined by charges on the atoms of the gramicidin A molecule, was obtained. The energy distribution and the wave functions for the stationary states of the ions were determined. The solutions of the Schrödinger equation for two conformers were compared.
