Title of article :
Proton transfer from exogenous donors in catalysis by human carbonic anhydrase II
Author/Authors :
Elder، نويسنده , , Ileana and Tu، نويسنده , , Chingkuang and Ming، نويسنده , , Li-June and McKenna، نويسنده , , Robert and Silverman، نويسنده , , David N.، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2005
Pages :
9
From page :
106
To page :
114
Abstract :
In the site-specific mutant of human carbonic anhydrase in which the proton shuttle His64 is replaced with alanine, H64A HCA II, catalysis can be activated in a saturable manner by the proton donor 4-methylimidazole (4-MI). From 1H NMR relaxivities, we found 4-MI bound as a second-shell ligand of the tetrahedrally coordinated cobalt in Co(II)-substituted H64A HCA II, with 4-MI located about 4.5 إ from the metal. Binding constants of 4-MI to H64A HCA II were estimated from: (1) NMR relaxation of the protons of 4-MI by Co(II)-H64A HCA II, (2) the visible absorption spectrum of Co(II)-H64A HCA II in the presence of 4-MI, (3) the inhibition by 4-MI of the catalytic hydration of CO2, and (4) from the catalyzed exchange of 18O between CO2 and water. These experiments along with previously reported crystallographic and catalytic data help identify a range of distances at which proton transfer is efficient in carbonic anhydrase II.
Keywords :
Isotope exchange , proton transfer , Carbon dioxide , magnetic resonance , carbonic anhydrase , enzyme activation
Journal title :
Archives of Biochemistry and Biophysics
Serial Year :
2005
Journal title :
Archives of Biochemistry and Biophysics
Record number :
1627207
Link To Document :
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