Literature DB >> 7848288

Measurement of the spin concentration of metalloprotein samples from saturation-magnetization data with particular reference to cytochrome c oxidase.

J Peterson1, E P Day, L L Pearce, M T Wilson.   

Abstract

A protocol for obtaining high-quality saturation-magnetization data from metalloprotein samples, employing a superconducting quantum interference device (SQUID) magnetometer, has previously been reported [E. P. Day, T. A. Kent, P. A. Lindahl, E. Münck, W. H. Orme-Johnson, H. Roder and A. Roy (1987) Biophys. J. 52, 837-853 and E. P. Day (1993) Methods Enzymol. 227, 437-463]. Following studies of several dozen different metalloprotein derivatives, the methodology has been further refined, particularly in the area of sample preparation. The details of the sample-handling procedures now in use are described, and moreover, the critical issue of verifying that contamination by paramagnetic impurities remains insignificant is considered. Importantly, it is shown that an independent determination of the quantity of paramagnetic sample present in the magnetometer is undesirable. Much more reliable parameters concerning the ground-state magnetic properties of the system under study are obtained if enough saturation-magnetization data are collected to enable the spin concentration to be determined during the subsequent fitting procedure. As proof of the validity of this method, the results of magnetization studies on ferricytochrome c, ferrocytochrome c and the benzohydroxamic acid adduct of horseradish peroxidase are presented. The ability of saturation-magnetization measurements to routinely determine spin concentration to within +/- 4% of accepted values is firmly established. In addition, a saturation-magnetization study has been performed on resting and fully reduced derivatives of cytochrome c oxidase. These results provide an illustration of the usefulness of the technique in probing some systems which have proved difficult to study by other methods. The increased difficulties inherent in obtaining meaningful data from these cytochrome c oxidase and other integer spin systems are delineated.

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Year:  1995        PMID: 7848288      PMCID: PMC1136340          DOI: 10.1042/bj3050871

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  22 in total

1.  Spectrum of horse-heart cytochrome c.

Authors:  E MARGOLIASH; N FROHWIRT
Journal:  Biochem J       Date:  1959-03       Impact factor: 3.857

2.  The magnetic susceptibility of cytochrome oxidase in the 4.2-1.5 K range.

Authors:  T H Moss; E Shapiro; T E King; H Beinert; C Hartzell
Journal:  J Biol Chem       Date:  1978-11-25       Impact factor: 5.157

3.  Magnetization of the sulfite and nitrite complexes of oxidized sulfite and nitrite reductases: EPR silent spin S = 1/2 states.

Authors:  E P Day; J Peterson; J J Bonvoisin; L J Young; J O Wilkerson; L M Siegel
Journal:  Biochemistry       Date:  1988-03-22       Impact factor: 3.162

4.  A plausible two-state model for cytochrome c oxidase.

Authors:  M T Wilson; J Peterson; E Antonini; M Brunori; A Colosimo; J Wyman
Journal:  Proc Natl Acad Sci U S A       Date:  1981-11       Impact factor: 11.205

5.  Magnetization and electron paramagnetic resonance studies of reduced uteroferrin and its "EPR-silent" phosphate complex.

Authors:  E P Day; S S David; J Peterson; W R Dunham; J J Bonvoisin; R H Sands; L Que
Journal:  J Biol Chem       Date:  1988-10-25       Impact factor: 5.157

6.  Cytochrome c oxidase binding of hydrogen peroxide.

Authors:  D Bickar; J Bonaventura; C Bonaventura
Journal:  Biochemistry       Date:  1982-05-25       Impact factor: 3.162

7.  Mössbauer and electron paramagnetic resonance studies of horseradish peroxidase and its catalytic intermediates.

Authors:  C E Schulz; R Rutter; J T Sage; P G Debrunner; L P Hager
Journal:  Biochemistry       Date:  1984-09-25       Impact factor: 3.162

8.  Antiferromagnetic exchange interaction in the two-iron-two-sulphur ferredoxin from the blue-green alga Spirulina maxima studied with a highly sensitive magnetic balance.

Authors:  L Petersson; R Cammack; K K Rao
Journal:  Biochim Biophys Acta       Date:  1980-03-26

9.  Endocytic mechanisms utilized by chlamydiae and their influence on induction of productive infection.

Authors:  D J Reynolds; J H Pearce
Journal:  Infect Immun       Date:  1991-09       Impact factor: 3.441

10.  Mössbauer, EPR, and magnetization studies of the Azotobacter vinelandii Fe protein. Evidence for a [4Fe-4S]1+ cluster with spin S = 3/2.

Authors:  P A Lindahl; E P Day; T A Kent; W H Orme-Johnson; E Münck
Journal:  J Biol Chem       Date:  1985-09-15       Impact factor: 5.157

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