Literature DB >> 6279655

Mechanism of autooxidation for hemoglobins and myoglobins. Promotion of superoxide production by protons and anions.

W J Wallace, R A Houtchens, J C Maxwell, W S Caughey.   

Abstract

Several hemoglobins and bovine myoglobin are shown to undergo autooxidation reactions promoted by anions. The reduced protein in the presence of oxygen and anion yields the anion complex of the oxidized (Met) species and a second product that is almost certainly superoxide. The second product can be detected by its reduction of cytochrome c3+ at the same rates and in the same amount as the Met species. Anions are increasingly effective as promoters in the same order as their strengths as nucleophiles, e.g. Cl- less than F- less than OCN- less than SCN- less than N3- less than CN-. Rates are directly proportional to anion concentrations. A linear dependence of rate upon [H+] is also observed and can be related to the protonation of a strongly acidic group. Globin from hemoglobin A and hemes with altered 2,4-substituents gave reconstituted hemoglobins that autooxidize at rates that decrease with the electron-withdrawing power of the substituent: acetyl greater than vinyl greater than hydrogen greater than ethyl. Changes in rate with globin structure can be interpreted in terms of steric access to the ligand binding site; the more sterically restricted is the site, the slower is the reaction. The effects of [O2] on the rate vary with the degree of saturation with O2. At high O2 levels (e.g. from saturation to the point where 5% deoxyHbA and 95% oxyHbA are present), a decrease in [O2] results in an increase in the rate of azide-promoted autooxidation. At O2 levels with from 5 to 75% deoxyHbA, the rate remains nearly constant. At still lower levels with oxyHbA less than 25%, the rate decreases as [O2] is lowered. Exposure to CO reduces the rate. The reaction mechanism for anion-induced autooxidation must provide for the stoichiometric formation of a cytochrome c3%-reducing species (presumably, superoxide), the anion acting as a nucleophile in the rate-determining step, the facilitation by protons, the sensitivity of the rate to the electronegativity of heme iron, and the varied effects of [O2] upon the rate. These findings can not be fully accommodated by mechanisms in which the Met species forms either via dissociative loss of superoxide from the oxy species followed by anion binding or via displacement of protonated dioxygen from oxyheme upon nucleophilic attack of the anion at heme iron. A consistent mechanism is the reaction of protonated deoxy species with the anion followed by the reaction of Fe2+-anion complex with O2 to give Fe3+-anion and (formula, see text). Here, the deoxy rather than oxy species is involved in Fe2+ oxidation to Fe3+; O2 can serve as one-electron acceptor but not while serving as an iron-bound ligand. A precise non-iron site for electron transfer from ferrous porphyrin to O2 remains unlocated but a process involving the porphyrin pi-system has analogy in simple heme, flavin, or other organic donor reactions with O2 that yield superoxide...

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Year:  1982        PMID: 6279655

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  37 in total

1.  Electrocatalytic O2-Reduction by Synthetic Cytochrome c Oxidase Mimics: Identification of a "Bridging Peroxo" Intermediate Involved in Facile 4e(-)/4H(+) O2-Reduction.

Authors:  Sudipta Chatterjee; Kushal Sengupta; Shabnam Hematian; Kenneth D Karlin; Abhishek Dey
Journal:  J Am Chem Soc       Date:  2015-09-30       Impact factor: 15.419

Review 2.  NO/redox disequilibrium in the failing heart and cardiovascular system.

Authors:  Joshua M Hare; Jonathan S Stamler
Journal:  J Clin Invest       Date:  2005-03       Impact factor: 14.808

3.  Oxidative modification by low levels of HOOH can transform myoglobin to an oxidase.

Authors:  Y Osawa; K Korzekwa
Journal:  Proc Natl Acad Sci U S A       Date:  1991-08-15       Impact factor: 11.205

4.  Direct measurement of nitrite transport across erythrocyte membrane vesicles using the fluorescent probe, 6-methoxy-N-(3-sulfopropyl) quinolinium.

Authors:  R Shingles; M H Roh; R E McCarty
Journal:  J Bioenerg Biomembr       Date:  1997-12       Impact factor: 2.945

Review 5.  Molecular controls of the oxygenation and redox reactions of hemoglobin.

Authors:  Celia Bonaventura; Robert Henkens; Abdu I Alayash; Sambuddha Banerjee; Alvin L Crumbliss
Journal:  Antioxid Redox Signal       Date:  2013-01-21       Impact factor: 8.401

6.  Interactions of Porphyromonas gingivalis with oxyhaemoglobin and deoxyhaemoglobin.

Authors:  John W Smalley; Andrew J Birss; Robert Withnall; Jack Silver
Journal:  Biochem J       Date:  2002-02-15       Impact factor: 3.857

7.  Accelerated autoxidation and heme loss due to instability of sickle hemoglobin.

Authors:  R P Hebbel; W T Morgan; J W Eaton; B E Hedlund
Journal:  Proc Natl Acad Sci U S A       Date:  1988-01       Impact factor: 11.205

8.  Lipid peroxidation and oxidation of several compounds by H2O2 activated metmyoglobin.

Authors:  J Kanner; S Harel
Journal:  Lipids       Date:  1985-09       Impact factor: 1.880

Review 9.  Metals and lipid oxidation. Contemporary issues.

Authors:  K M Schaich
Journal:  Lipids       Date:  1992-03       Impact factor: 1.880

10.  Current Challenges in the Development of Acellular Hemoglobin Oxygen Carriers by Protein Engineering.

Authors:  Andres S Benitez Cardenas; Premila P Samuel; John S Olson
Journal:  Shock       Date:  2019-10       Impact factor: 3.454

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