Literature DB >> 901910

Mössbauer and susceptibility experiments on different compounds of Fe3+-myoglobin.

U F Thomanek, F Parak, S Formanek, G M Kalvius.   

Abstract

The static magnetic susceptibilities of different ferric high spin and low spin compounds of myoglobin (Mb(H2O), Mb(H2O) frozen under high pressure, MbF, MbCN) were measured in the temperature region between 4.2 K and 130 K. Mössbauer absorption experiments on Mb(H2O) and MbF were performed at different temperatures between 4.2 K and 180 K and in small magnetizing fields H less than or equal to 1 kOe. The evaluation of our experimental data was performed with a Hamiltonian describing of 3d-configuration of the ferric iron by taking into account the Coulomb repulsion of the five electrons within the 3d-shell, the crystal electric field of C2v-symmetry, and the spine-orbit coupling. The Hamiltonian contains the splitting energies of the five antibonding d-orbitals (dxy, dx2, dy2, dx2-y2, dz2) as parameters. The values of these energies were obtained by a least squares fitting procedure using our magnetic susceptibility data together with the g-factors taken from the literature. In the case of MbF the energy difference between the two lowest Kramers doublets was also determined from present Mössbauer data. The results of the susceptibility and the Mössbauer data are in good agreement. The splitting energies of the 3d-orbitals can be correlated to the distances between the iron and its nearest neighbours. The different positions of the iron in the compounds investigated are discussed.

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Year:  1977        PMID: 901910     DOI: 10.1007/bf00535697

Source DB:  PubMed          Journal:  Biophys Struct Mech        ISSN: 0340-1057


  14 in total

1.  A MAGNETOCHEMICAL STUDY OF EQUILIBRIA BETWEEN HIGH AND LOW SPIN STATES OF METMYOGLOBIN COMPLEXES.

Authors:  J BEETLESTONE; P GEORGE
Journal:  Biochemistry       Date:  1964-05       Impact factor: 3.162

2.  A spectrophotometric method for the simultaneous determination of myoglobin and hemoglobin in extracts of human muscle.

Authors:  C DE DUVE
Journal:  Acta Chem Scand       Date:  1948

3.  Influence of globin structure on the state of the heme. 3. Changes in heme spectra accompanying allosteric transitions in methemoglobin and their implications for heme-heme interaction.

Authors:  M F Perutz; E J Heidner; J E Ladner; J G Beetlestone; C Ho; E F Slade
Journal:  Biochemistry       Date:  1974-05-07       Impact factor: 3.162

4.  Electron paramagnetic resonance (34 and 55 GHz) studies of hemoproteins.

Authors:  A L Gray; H A Buckmaster
Journal:  Can J Biochem       Date:  1973-08

5.  Magnetic susceptibility measurements on hemoproteins down to 4.2 degrees K.

Authors:  A Tasaki; J Otsuka; M Kotani
Journal:  Biochim Biophys Acta       Date:  1967-06-27

6.  Magnetic anisotropy of the myoglobin single crystal.

Authors:  H Morimoto; T Iizuka; J Otsuka; M Kotani
Journal:  Biochim Biophys Acta       Date:  1965-07-22

7.  Influence of globin structure on the state of the heme. II. Allosteric transitions in methemoglobin.

Authors:  M F Perutz; A R Fersht; S R Simon; G C Roberts
Journal:  Biochemistry       Date:  1974-05-07       Impact factor: 3.162

8.  Stereochemistry of cooperative effects in haemoglobin.

Authors:  M F Perutz
Journal:  Nature       Date:  1970-11-21       Impact factor: 49.962

9.  Electronic structure and quadrupole splittings of ferrous iron in hemoglobin.

Authors:  H Eicher; A Trautwein
Journal:  J Chem Phys       Date:  1969-03-15       Impact factor: 3.488

10.  Electronic structure and spatial arrangement of C2v-coordinated ferric iron in metmyoglobin, metmyoglobin fluoride, and methemoglobin.

Authors:  H Eicher
Journal:  Z Naturforsch C Biosci       Date:  1975 Nov-Dec
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  2 in total

1.  Distinct reaction pathways followed upon reduction of oxy-heme oxygenase and oxy-myoglobin as characterized by Mössbauer spectroscopy.

Authors:  Ricardo Garcia-Serres; Roman M Davydov; Toshitaka Matsui; Masao Ikeda-Saito; Brian M Hoffman; Boi Hanh Huynh
Journal:  J Am Chem Soc       Date:  2007-02-07       Impact factor: 15.419

2.  Experimental and theoretical characterization of the high-affinity cation-binding site of the purple membrane.

Authors:  L Pardo; F Sepulcre; J Cladera; M Duñach; A Labarta; J Tejada; E Padrós
Journal:  Biophys J       Date:  1998-08       Impact factor: 4.033

  2 in total

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