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J. Biol. Chem., Vol. 261, Issue 18, 8204-8212, 06, 1986
Ions binding to S100 proteins. II. Conformational studies and calcium- induced conformational changes in S100 alpha alpha protein: the effect of acidic pH and calcium incubation on subunit exchange in S100a (alpha beta) protein
J Baudier and D Gerard
A rapid separation method for bovine brain S100 alpha alpha, S100a, and
S100b protein using fast protein liquid chromatography on a Mono Q column
and its application in preparation of a large amount of S100 alpha alpha
protein are described. The conformation of S100 alpha alpha in the
metal-free forms as well as in the presence of calcium were studied by UV
absorption, circular dichroism, intrinsic fluorescence, sulfhydryl
reactivity, and interaction with a hydrophobic fluorescent probe. The
alpha-subunit appears to have nearly identical conformation in S100 alpha
alpha and S100a protein dimers. We also confirmed that only the
alpha-subunit exposes hydrophobic domains to solvent in the presence of
calcium and that cysteine residues exposed upon Ca2+ binding to S100
proteins correspond to Cys 85 alpha and Cys 84 beta. Incubation of S100a
with calcium and KCl proved that calcium binding to the putative
calcium-binding sites (site I alpha, I beta) triggers a time- and
temperature-dependent conformational change in the protein structure which
decreases the antagonistic effect of KCl on calcium binding to sites II
alpha and II beta and provokes subunit exchanges between protein dimers and
the emergence of S100 alpha alpha and S100b (beta beta) proteins. Dynamic
fluorescence measurements showed that incubating calcium at high S100a
protein concentrations (greater than 10(-5) M) induces an apparent slow
dimer-monomer equilibrium which might result in total subunit dissociation
at lower protein concentrations. The effect of acidic pH on subunit
dissociation in S100a protein (Morero, R. D., and Weber, G. (1982) Biochim.
Biophys. Acta 703, 231-240) arises from conformational changes in the
protein structure that are similar to those induced by Ca2+ incubation.

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Copyright © 1986 by the American Society for Biochemistry and Molecular Biology.
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