The gating polarizational currents were computed on the basis of the dipole moment changes occurring in nerve membrane ionic channel subunits. Membrane thickness and surface density of channels were the only parameters used in addition to the Hodgkin-Huxley model. The gating currents computed for membrane potentials where the Hodgkin-Huxley empirical formulae are reliable were found to be in good agreement with the available experimental data. It is demonstrated that the gating currents of the n and h subunits are responsible for the late slowly decaying gating currents
An integral representation for the membrane admittance in terms of its known current response to a v...
We have approached the problem of nerve excitability through three questions: (a) What is the diagra...
Two illustrative molecular models, designed to explain the Cole-Moore K+ hyperpolarization delay, ar...
It has been repeatedly noted that the change of conformation of the molecules that serve as the ion-...
Dipole moment, enthalpy, and entropy changes were calculated for hypothetical structural units which...
Steady-state and kinetic properties of gating currents of the Shaker K+ channels were studied in cha...
Internally perfused and pronase-treated giant axons were prepared for gating current measurements. G...
A structural model is suggested for axon membranes consisting of a double layer of lipid and phospho...
A kinetic model of sodium activation gating is presented. The kinetics are based on harmonic analysi...
The Hodgkin-Huxley equations, originally developed to describe the electrical events in the squid gi...
The enzyme model of the nerve [11] is analyzed numerically and it is shown that with a suitable choi...
We have developed a novel technique for simulating the influence of the effects of single channel ki...
Using Stern's double-layer adsorption model for the density of cations in the membrane pores, a quan...
The change in capacity of squid axon membrane during hyper- and depolarizations was investigated in ...
Voltage-clamped squid giant axons, perfused internally and ex-ternally with solutions containing 10-...
An integral representation for the membrane admittance in terms of its known current response to a v...
We have approached the problem of nerve excitability through three questions: (a) What is the diagra...
Two illustrative molecular models, designed to explain the Cole-Moore K+ hyperpolarization delay, ar...
It has been repeatedly noted that the change of conformation of the molecules that serve as the ion-...
Dipole moment, enthalpy, and entropy changes were calculated for hypothetical structural units which...
Steady-state and kinetic properties of gating currents of the Shaker K+ channels were studied in cha...
Internally perfused and pronase-treated giant axons were prepared for gating current measurements. G...
A structural model is suggested for axon membranes consisting of a double layer of lipid and phospho...
A kinetic model of sodium activation gating is presented. The kinetics are based on harmonic analysi...
The Hodgkin-Huxley equations, originally developed to describe the electrical events in the squid gi...
The enzyme model of the nerve [11] is analyzed numerically and it is shown that with a suitable choi...
We have developed a novel technique for simulating the influence of the effects of single channel ki...
Using Stern's double-layer adsorption model for the density of cations in the membrane pores, a quan...
The change in capacity of squid axon membrane during hyper- and depolarizations was investigated in ...
Voltage-clamped squid giant axons, perfused internally and ex-ternally with solutions containing 10-...
An integral representation for the membrane admittance in terms of its known current response to a v...
We have approached the problem of nerve excitability through three questions: (a) What is the diagra...
Two illustrative molecular models, designed to explain the Cole-Moore K+ hyperpolarization delay, ar...