Literature DB >> 10648142

A new method for quantitation of spin concentration by EPR spectroscopy: application to methemoglobin and metmyoglobin.

D A Svistunenko1, M A Sharpe, P Nicholls, M T Wilson, C E Cooper.   

Abstract

A new method of EPR spectral analysis is developed to quantitate overlapping signals. The method requires double integration of a number of spectra containing the signals in different proportions and the subsequent solution of a system of linear equations. The result gives the double integral values of the individual lines, which can then be further used to find the concentrations of all the paramagnetic species present. There is no requirement to deconvolute the whole spectrum into its individual components. The method is employed to quantify different heme species in methemoglobin and metmyoglobin preparations. A significantly greater intensity of the high-spin signal in metmyoglobin, compared to methemoglobin at the same heme concentration, is shown to be due to larger amounts of low-spin forms in methemoglobin. Three low-spin types in methemoglobin and two in metmyoglobin are present in these samples. When their calculated concentrations are added to those of the high-spin forms, the results correspond to the total heme concentrations obtained by optical spectroscopy. Copyright 2000 Academic Press.

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Year:  2000        PMID: 10648142     DOI: 10.1006/jmre.1999.1935

Source DB:  PubMed          Journal:  J Magn Reson        ISSN: 1090-7807            Impact factor:   2.229


  6 in total

1.  Comparative study of tyrosine radicals in hemoglobin and myoglobins treated with hydrogen peroxide.

Authors:  Dimitri A Svistunenko; Jacqueline Dunne; Michael Fryer; Peter Nicholls; Brandon J Reeder; Michael T Wilson; Maria Giulia Bigotti; Francesca Cutruzzolà; Chris E Cooper
Journal:  Biophys J       Date:  2002-11       Impact factor: 4.033

2.  Axial coordination of heme in ferric CcmE chaperone characterized by EPR spectroscopy.

Authors:  Inés García-Rubio; Martin Braun; Igor Gromov; Linda Thöny-Meyer; Arthur Schweiger
Journal:  Biophys J       Date:  2006-12-01       Impact factor: 4.033

3.  The pH dependence of naturally occurring low-spin forms of methaemoglobin and metmyoglobin: an EPR study.

Authors:  D A Svistunenko; M A Sharpe; P Nicholls; C Blenkinsop; N A Davies; J Dunne; M T Wilson; C E Cooper
Journal:  Biochem J       Date:  2000-11-01       Impact factor: 3.857

4.  Covalent modifications of hemoglobin by nitrite anion: formation kinetics and properties of nitrihemoglobin.

Authors:  Mai Otsuka; Sarah A Marks; Daniel E Winnica; Andrew A Amoscato; Linda L Pearce; Jim Peterson
Journal:  Chem Res Toxicol       Date:  2010-10-20       Impact factor: 3.739

5.  Ascorbate removes key precursors to oxidative damage by cell-free haemoglobin in vitro and in vivo.

Authors:  Jacqueline Dunne; Alexis Caron; Patrick Menu; Abdu I Alayash; Paul W Buehler; Michael T Wilson; Radu Silaghi-Dumitrescu; Beatrice Faivre; Chris E Cooper
Journal:  Biochem J       Date:  2006-11-01       Impact factor: 3.857

6.  The mechanism of formation, structure and physiological relevance of covalent hemoglobin attachment to the erythrocyte membrane.

Authors:  Elizabeth M Welbourn; Michael T Wilson; Ashril Yusof; Metodi V Metodiev; Chris E Cooper
Journal:  Free Radic Biol Med       Date:  2016-12-20       Impact factor: 7.376

  6 in total

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