Theory of 14 N and 17 O Nuclear Quadrupole Interactions in the Single Amino Acids Occurring in the Protein Chain of Cytochrome c

The understanding of electron transport in proteins based on a novel technique involving muon spin rotation (μSR)measurements is a topic of great current interest. The technique, which involves study of spin relaxation of a positive muon (μ + ) trapped in amino acids in protein chains due to the fluctuating magnetic field that the moving electron produces, is based on the premise that the electron is generated by ionization of a muonium (Mu) which was trapped at the same site as the μ + left behind. In attempting to test this premise from first-principles for the Cytochrome c (Cyt c) system in which recent μSR measurements have been made, we have carried out Hartree- Fock investigations of the electronic structures of the bare amino acids and amino acids with + and Mu trapped at the oxygen of the C=O group common to all amino acids. With the aim that the comparison of theoretically predicted experimental nuclear quadrupole interaction (NQI) parameters will provide a useful test of the electron distribution in the amino acids of Cyt c, we present results for the nuclear quadrupole coupling constants (e 2 qQ) and asymmetry parameters (η) for the bare amino acids and the amino acids with trapped μ + and Mu. The trends in 2 and for 14 N and 17 O between the various amino acids, as well as the changes in these parameters in the presence of μ + and Mu are being analyzed. It would be helpful to have experimental data for e 2 qQ and to η compare with our predictions for the amino acids as they occur in vitro in polycrystalline Cyt c in which the SR measurements have been carried out. It is also hoped that the μSR technique will be able to provide experimental data on e 2 qQ and for the 14 N and 17 O nuclei to compare with our predictions