Voltage-gated ion channels are found in many membrane-enclosed structures, including synaptic vesicles, endosomes, mitochondria, chloroplasts, viruses and bacteria. In small compartments, assumptions underlying Hodgkin-Huxley-type models must be relaxed: 1 stochastic gating of individual ion channels can substantially change the membrane voltage, even during a single gating event; and 2 ionic currents, even through a single channel, can substantially alter internal ionic concentrations. We adapted conductance-based models to incorporate these effects, and we then simulated voltage dynamics of small vesicles as a function of vesicle radius and channel density. We identified regimes in this parameter space with qualitatively distinct dynamics. We then performed stochastic simulations to explore the role of NaV1.5 in maturation of macrophage endosomes. The stochastic model predicted dramatically different dynamics compared to a classical conductance-based approach. Electrophysiology of small structures can be very different from larger structures, even when ion channel composition and density are preserved.
Howell et al. (Thu,) studied this question.