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Validity of the rapid buffering approximation near a point source of calcium ions.

, , and . Biophys. J., 70 (6): 2527--2539 (June 1996)

Abstract

In the presence of rapid buffers the full reaction-diffusion equations describing Ca$^2+$ transport can be reduced using the rapid buffering approximation to a single transport equation for Ca$^2+$. Here we simulate the full and reduced equations, exploring the conditions necessary for the validity of the rapid buffering approximation for an isolated Ca$^2+$ channel or a cluster of channels. Using a point source and performing numerical simulations of different durations, we quantify the error of the rapid buffering approximation as a function of buffer and source parameters as well as the time and spatial scale set by the resolution of confocal microscopic measurements. We carry out simulations of Ca$^2+$ "sparks" and "puffs," both with and without the indicator dye Ca$^2+$ Green-1, and find that the rapid buffering approximation is excellent. These calculations also show that the traditional calculation of Ca$^2+$ from a fluorescence signal may grossly underestimate the true value of Ca$^2+$ near a source. Finally, we use the full model to simulate the transient Ca$^2+$ domain near the pore of an open Ca$^2+$ channel in a cell dialyzed with millimolar concentrations of 1,2-bis(2-aminophenoxy)ethane-N,N,N,N-tetraacetic acid or EGTA. In this regime, where the rapid buffering approximation is poor. Neher's equation for the steady-state Ca$^2+$ profile is shown to be a reliable approximation adjacent to the pore.

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