The complexing properties of the sub-isoforms of several mammalian Zn-conta
ining metallothioneins (ZnMT) from different origins (rat, rabbit and human
foetal livers) have been investigated by capillary zone electrophoresis co
upled to diode array detection (CZE-DAD). MTs were submitted to three diffe
rent experiments: gradual additions of Cd to MT at PH 8.0, variation of the
pH and addition of Cd followed by a variation of the pH. On the whole ther
e seems to he no displacement of the zinc originally present in the MT, but
incorporation of Cd in the molecule in order to reach saturation. Furtherm
ore, the pH variations allow one to conclude a certain reversibility of the
system. All these results confirm those previously obtained by differentia
l pulse polarography (DPP). The procedure used in this work shows that the
sub-isoforms of an MT may exhibit variable complexing properties. This is p
articularly well illustrated in the case of rat liver MT-2. Much likely the
re are different mixed complexes of Cd and Zn in each sub-isoform, forming
various metalloforms. This work illustrates a different and original use of
CZE-DAD for studying the complexing properties of metal-binding proteins.
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