Abstract
Brownian ratchet like stochastic theory for the electrochemical membrane system of Hodgkin-Huxley (HH) is developed. The system is characterized by a continuous variable , representing mobile membrane charge density, and a discrete variable representing ion channel conformational dynamics. A Nernst-Planck-Nyquist-Johnson type equilibrium is obtained when multiple conducting ions have a common reversal potential. Detailed balance yields a previously unknown relation between the channel switching rates and membrane capacitance, bypassing Eyring-type explicit treatment of gating charge kinetics. From a molecular structural standpoint, membrane charge is a more natural dynamic variable than potential ; our formalism treats -dependent conformational transition rates as intrinsic parameters. Therefore in principle, vs. is experimental protocol dependent,e.g., different from voltage or charge clamping measurements. For constant membrane capacitance per unit area and neglecting membrane potential induced by gating charges, , and HH's formalism is recovered. The presence of two types of ions, with different channels and reversal potentials, gives rise to a nonequilibrium steady state with positive entropy production . For rapidly fluctuating channels, an expression for is obtained.
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