Literature DB >> 6266527

Proton magnetic relaxation dispersion in solutions of the cuproprotein diamine oxidase.

M D Kluetz, P G Schmidt.   

Abstract

Proton nuclear magnetic resonance relaxation measurements were made over the range 4.7--220 MHz for aqueous solutions of hog kidney diamine oxidase. The values of 1/T1 give rise in two distinct dispersions, at 16 and 75 MHz, whereas 1/T2 displays a minimum at 20 MHz. The temperature dependence of relaxation rates in all cases yield apparent activation energies less than 0.6 kcal/mol. These data indicate to us that the two Cu(II) ions of diamine oxidase are intrinsically different in terms of their electronic relaxation characteristics and hence, chemical environments. Low field limits of the two electronic relaxation times are 2 and 10 ns, with one of these correlation times being frequency dependent. The value of the frequency-dependent electronic relaxation time is governed by interactions that are modulated by a process having a correlation time of 5 ps.

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Year:  1980        PMID: 6266527      PMCID: PMC1328697          DOI: 10.1016/S0006-3495(80)85132-0

Source DB:  PubMed          Journal:  Biophys J        ISSN: 0006-3495            Impact factor:   4.033


  5 in total

1.  Anomalous relaxation of water protons in solutions of copper-containing proteins.

Authors:  S H Koenig; R D Brown
Journal:  Ann N Y Acad Sci       Date:  1973-12-31       Impact factor: 5.691

Review 2.  Contributions of EPR spectroscopy to our knowledge of oxidative enzymes.

Authors:  H Beinert; G Palmer
Journal:  Adv Enzymol Relat Areas Mol Biol       Date:  1965

3.  Nuclear magnetic relaxation dispersion in protein solutions. V. Bovine erythrocyte superoxide dismutase.

Authors:  B P Gaber; R D Brown; S H Koenig; J A Fee
Journal:  Biochim Biophys Acta       Date:  1972-06-22

4.  Diamine oxidase: molecular weight and subunit analysis.

Authors:  M D Kluetz; P G Schmidt
Journal:  Biochem Biophys Res Commun       Date:  1977-05-09       Impact factor: 3.575

5.  Proton relaxation study of the hog kidney diamine oxidase active center.

Authors:  M D Kluetz; P G Schmidt
Journal:  Biochemistry       Date:  1977-11-29       Impact factor: 3.162

  5 in total

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