The peculiarity of ion transport at the nanoscale is revealed through electrophysiological studies of two biological ion channels: the cation-selective bacterial porin-OmpF and the mitochondrial voltage-dependent anion channel (VDAC). We provide evidence of an unprecedented scaling behavior in the power-law relationship between conductivity and concentration G ∼ c α with α > 1 when functional groups attached to the pore inner wall have opposite charges to those located in the nanochannel's outer surface. Indeed, we find α ∼ 1.4 both for OmpF in positively charged membranes and for VDAC in negatively charged ones. The experiments are analyzed using different levels of theoretical models, starting with an equivalent circuit where total electrical current is described as the sum of ionic currents. Subsequently, we show that electrical circuits incorporating simplifying assumptions such as local electroneutrality and Donnan equilibrium consistently account for the measured G-c relationships yielding extremely similar results to the numerical results of structure-based Poisson-Nernst-Planck equations computed without these assumptions. We demonstrate that unexpected scaling exponents do not correspond to deviations from these classical equilibrium/electroneutrality assumptions, but rather to the structural features of the pore that are not included in oversimplified models in terms of shape and/or charge distribution. In contrast to the predictions of widely accepted models, we demonstrate both experimentally and theoretically that the conductance of ion-selective nanochannels can be drastically reduced in dilute solutions through a mechanism in which membrane charges and pore charges do not compensate for each other but act as interacting sites of opposite charge. Our insights into the critical role of external surface charges aim to open new conceptual avenues for developing nanofluidic devices with enhanced capabilities for energy conversion and sensing properties.
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