The thermodynamics and kinetics of the weakly electron-coupled proton transfer of Pseudomonas aeruginosa azurin have been studied and quantitatively determined using fast scan cyclic voltammetry (CV), in which the protein is adsorbed on two types of electrode (pyrolytic graphite 'edge' (PGE) or 1-decanethiol modified gold). Electron transfer is coupled to a slow protonation of His35, which is not a ligand to the copper ion but is located approximately 8 Å away. Protonation of His35 produces small changes in the reduction potential of the copper site, which are time-resolved within the scan rate range 0.01-100 V s-1. © 2002 Elsevier Science B.V. All rights reserved
Type zero copper is a hard-ligand analogue of the classical type 1 or blue site in copper proteins t...
The interaction between azurin from Pseudomonas aeruginosa and Ag(I), Cu(II), Hg(II), was investigat...
AbstractSite-directed mutagenesis of the structural gene for azurin from Pseudomonas aeruginosa has ...
The ionic strength (I) dependence of the reduction thermodynamics (E\ub0\u2032, \u394Hrc\ub0\u2032, ...
The hydrophobic patch of azurin (AZ)from Pseudomonas aeruginosa is an important recognitionsurface f...
The rapid electron-transfer reaction of the blue copper protein azurin adsorbed on different electro...
In the hydrophobic patch of azurin from Pseudomonas aeruginosa, an electric dipole was created by ch...
We are investigating interfacial electron transfer rates of P. aeruginosa azurin and its mutants usi...
A study of the pH and temperature dependence of the redox potentials of azurins from five species of...
The hydrophobic patch of azurin (AZ) from <i>Pseudomonas aeruginosa</i> is an important recognition ...
Well-defined voltammetric responses of redox proteins with acidic-to-neutral pI values have been obt...
Long-range electron transfer (ET) reactions are central to many biochemical processes. To accomplish...
Abstract The kinetics of electron transfer between the copper-containing protein azurin (Cu++/Cu+) a...
<i>Pseudomonas aeruginosa</i> azurin has been an important model system for investigating fundamenta...
(Figure Presented) Variations in the formal electrochemical potential (E 0) ...
Type zero copper is a hard-ligand analogue of the classical type 1 or blue site in copper proteins t...
The interaction between azurin from Pseudomonas aeruginosa and Ag(I), Cu(II), Hg(II), was investigat...
AbstractSite-directed mutagenesis of the structural gene for azurin from Pseudomonas aeruginosa has ...
The ionic strength (I) dependence of the reduction thermodynamics (E\ub0\u2032, \u394Hrc\ub0\u2032, ...
The hydrophobic patch of azurin (AZ)from Pseudomonas aeruginosa is an important recognitionsurface f...
The rapid electron-transfer reaction of the blue copper protein azurin adsorbed on different electro...
In the hydrophobic patch of azurin from Pseudomonas aeruginosa, an electric dipole was created by ch...
We are investigating interfacial electron transfer rates of P. aeruginosa azurin and its mutants usi...
A study of the pH and temperature dependence of the redox potentials of azurins from five species of...
The hydrophobic patch of azurin (AZ) from <i>Pseudomonas aeruginosa</i> is an important recognition ...
Well-defined voltammetric responses of redox proteins with acidic-to-neutral pI values have been obt...
Long-range electron transfer (ET) reactions are central to many biochemical processes. To accomplish...
Abstract The kinetics of electron transfer between the copper-containing protein azurin (Cu++/Cu+) a...
<i>Pseudomonas aeruginosa</i> azurin has been an important model system for investigating fundamenta...
(Figure Presented) Variations in the formal electrochemical potential (E 0) ...
Type zero copper is a hard-ligand analogue of the classical type 1 or blue site in copper proteins t...
The interaction between azurin from Pseudomonas aeruginosa and Ag(I), Cu(II), Hg(II), was investigat...
AbstractSite-directed mutagenesis of the structural gene for azurin from Pseudomonas aeruginosa has ...