ELECTRON SPIN ECHO MODULATION OF DEOXYCO MYOGLOBIN & DEOXYCO PORPHYRIN MODELS

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Electron spin echo modulation spectra were recorded for the blue copper protein rusticyanin and a mutant lacking one of the two histidine ligands to copper (H85A). The w.t. and H85A forms of the protein were examined in depth to fully characterize the ESEEM spectroscopic properties of imidazole nitrogens in the copper ligand field. The use of timing variables (tau selection) in the three pulse experiment as a means to identify peaks has been established. A graphical method of identifying peaks and quantifying superhyperfine parameters from experimental data has also been demonstrated. The ESEEM spectra suggest that m=1 transitions of both spin manifolds may be observed by a judicious choice of tau in a three pulse experiment. This greatly improves the accuracy of the simulation process and removes ambiguity in misidentifying peaks by an improper association. A graphical representation of the peaks allows one to predict the condition of "exact cancellation" and thereby remove ambiguities in quantifying the superhyperfine parameters. Further, the absence of the second histidine ligand puts more spin density onto the remaining histidine ligand to copper. Paper has been published based on this