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Biophys J, October 2000, p. 1976-1992, Vol. 79, No. 4
*Department of Physiology and Biophysics, University of Miami
School of Medicine, Miami, Florida 33101-4819; and
Department of Molecular Biophysics and Physiology, Rush
Medical College, Chicago, Illinois 60612 USA
L-type calcium channels are Ca2+ binding
proteins of great biological importance. They generate an essential
intracellular signal of living cells by allowing Ca2+ ions
to move across the lipid membrane into the cell, thereby selecting an
ion that is in low extracellular abundance. Their mechanism of
selection involves four carboxylate groups, containing eight oxygen
ions, that belong to the side chains of the "EEEE" locus of the
channel protein, a setting similar to that found in many
Ca2+-chelating molecules. This study examines the
hypothesis that selectivity in this locus is determined by mutual
electrostatic screening and volume exclusion between ions and
carboxylate oxygens of finite diameters. In this model, the eight
half-charged oxygens of the tethered carboxylate groups of the protein
are confined to a subvolume of the pore (the "filter"), but
interact spontaneously with their mobile counterions as ions interact
in concentrated bulk solutions. The mean spherical approximation (MSA)
is used to predict ion-specific excess chemical potentials in the
filter and baths. The theory is calibrated using a single experimental observation, concerning the apparent dissociation constant of Ca2+ in the presence of a physiological concentration of
NaCl. When ions are assigned their independently known crystal
diameters and the carboxylate oxygens are constrained, e.g., to a
volume of 0.375 nm3 in an environment with an effective
dielectric coefficient of 63.5, the hypothesized selectivity filter
produces the shape of the calcium binding curves observed in
experiment, and it predicts Ba2+/Ca2+ and
Na+/Li+ competition, and Cl
exclusion as observed. The selectivities for Na+,
Ca2+, Ba2+, other alkali metal ions, and
Cl
thus can be predicted by volume exclusion and
electrostatic screening alone. Spontaneous coordination of ions and
carboxylates can produce a wide range of Ca2+
selectivities, depending on the volume density of carboxylate groups
and the permittivity in the locus. A specific three-dimensional structure of atoms at the binding site is not needed to explain Ca2+ selectivity.
Biophys J, October 2000, p. 1976-1992, Vol. 79, No. 4
© 2000 by the Biophysical Society 0006-3495/00/10/1976/17 $2.00
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