Cu,Zn superoxide dismutases are characterized by the presence of four highly conserved charged residues (Lys120, Glu/Asp130, Glu131 and Lys134), which are placed at the edge of the active site channel and have been shown to be individually involved in the electrostatic attraction of the substrate toward the catalytically active copper ion. By genetic engineering we mutated these four residues into neutrally charged ones (Leu120, Gln130, Gln131, Thr134). The effects of these mutations on the rate of superoxide dismutation were not dramatic. In fact, at two different pH and ionic strength values, the mutant enzyme had a catalytic constant. even higher with respect to the wild-type protein, showing that electrostatic interaction at these surface sites is not essential for high catalytic efficiency of the enzyme. The mutant and the wild-type enzyme showed the same degree of inhibition by CN-, and both were not affected by I-, showing that mutations did not alter the sensitivity of the enzyme to anions. On the other hand, reconstitution of active enzyme from either the wild-type or mutant copper-free enzymes with a copper(I)glutathione [Cu(I)-GSH] complex showed that metal uptake by the mutant was much slower than by the wildtype enzyme. The demonstration that the 'electrostatic loop' is apparently conserved to assure optimal copper uptake by the enzyme, rather than fast dismutation, may provide further support to the idea that Cu,Zn superoxide dismutase is a bifunctional protein, acting in cellular defense against oxidative stress both as a copper buffer and as a superoxide radical scavenger.

Ciriolo, M., Battistoni, A., Falconi, M., Filomeni, G., Rotilio, G. (2001). Role of the electrostatic loop of Cu,Zn superoxide dismutase in the copper uptake process. EUROPEAN JOURNAL OF BIOCHEMISTRY, 268(3), 737-742 [10.1046/j.1432-1327.2001.01928.x].

Role of the electrostatic loop of Cu,Zn superoxide dismutase in the copper uptake process

Ciriolo MR;Battistoni A;Falconi M;Filomeni G;Rotilio G
2001-01-01

Abstract

Cu,Zn superoxide dismutases are characterized by the presence of four highly conserved charged residues (Lys120, Glu/Asp130, Glu131 and Lys134), which are placed at the edge of the active site channel and have been shown to be individually involved in the electrostatic attraction of the substrate toward the catalytically active copper ion. By genetic engineering we mutated these four residues into neutrally charged ones (Leu120, Gln130, Gln131, Thr134). The effects of these mutations on the rate of superoxide dismutation were not dramatic. In fact, at two different pH and ionic strength values, the mutant enzyme had a catalytic constant. even higher with respect to the wild-type protein, showing that electrostatic interaction at these surface sites is not essential for high catalytic efficiency of the enzyme. The mutant and the wild-type enzyme showed the same degree of inhibition by CN-, and both were not affected by I-, showing that mutations did not alter the sensitivity of the enzyme to anions. On the other hand, reconstitution of active enzyme from either the wild-type or mutant copper-free enzymes with a copper(I)glutathione [Cu(I)-GSH] complex showed that metal uptake by the mutant was much slower than by the wildtype enzyme. The demonstration that the 'electrostatic loop' is apparently conserved to assure optimal copper uptake by the enzyme, rather than fast dismutation, may provide further support to the idea that Cu,Zn superoxide dismutase is a bifunctional protein, acting in cellular defense against oxidative stress both as a copper buffer and as a superoxide radical scavenger.
Pubblicato
Rilevanza internazionale
Articolo
Sì, ma tipo non specificato
Settore BIO/10
English
Con Impact Factor ISI
Copper; Electrostatic loop; Superoxide dismutase
Ciriolo, M., Battistoni, A., Falconi, M., Filomeni, G., Rotilio, G. (2001). Role of the electrostatic loop of Cu,Zn superoxide dismutase in the copper uptake process. EUROPEAN JOURNAL OF BIOCHEMISTRY, 268(3), 737-742 [10.1046/j.1432-1327.2001.01928.x].
Ciriolo, M; Battistoni, A; Falconi, M; Filomeni, G; Rotilio, G
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/55108
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