Title of article
Differences between Mg2+ and Transition Metal Ions in the Activation of Calcineurin
Author/Authors
Martin، نويسنده , , Bruce L. and Li، نويسنده , , Baitao and Liao، نويسنده , , Chuxiong and Rhode، نويسنده , , David J.، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2000
Pages
7
From page
71
To page
77
Abstract
Exogenous metal ion activation of calcineurin catalyzed hydrolysis of para-nitrophenyl phosphate was kinetically characterized at 20, 25, 30, and 37°C. Analysis yielded estimates for thermodynamic parameters for the activation of calcineurin by each of the metal ions. Values for ΔGMe° were varied with the best activators resulting in more stable enzyme–metal ion complexes and with ΔGMe° dominated by the entropic component. Mg2+ was the only nontransition metal ion which supported significant activity and showed some distinct characteristics including a negative ΔSMe°, suggesting that activation by Mg2+ may have resulted in a unique enzyme–metal ion form. Circular dichroism showed that metal ions increased the α-helical content of calcineurin, but little significant differences in the spectra were identified between using activating and nonactivating metal ions. Activating Mg2+, but not nonactivating Ca2+, did cause changes in the Fourier transform infrared photoacoustic spectrum of calcineurin compared to the spectrum of calcineurin with Mn2+. Other metal ions, Co2+ and Ni2+, also caused no changes in the infrared spectrum. Possible explanations for these differences between Mg2+ and transition metal ions in the activation of calcineurin are discussed.
Journal title
Archives of Biochemistry and Biophysics
Serial Year
2000
Journal title
Archives of Biochemistry and Biophysics
Record number
1616923
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