Literature DB >> 6256734

Ion-transport chain of cytochrome oxidase: the two chain-direct coupling principle of energy coupling.

M Fry, D E Green.   

Abstract

Cytochrome oxidase (ferrocytochrome c:oxygen oxidoreductase, EC 1.9.3.1) couples the aerobic oxidation of ferrocytochrome c to the cyclical transport of monovalent cations or to the active transport of monovalent and divalent cations. This transport capability is mediated by an intracomplex ion-transport chain of two protein-bound molecules of cardiolipin per molecule of cytochrome oxidase. Cardiolipin in a two-phase system shows the identical ionophoric pattern as does the cytochrome oxidase coupled system. A molecular model of the cardiolipin chain suggests the possibility of a cage-like structure through which cations can be transferred from phosphate group to phosphate group. The ion-transport chain and the electron-transport chain are anchored to the same set of subunits (I+IV); the close proximity of the two chains argues for the direct coupling of electron and cation flow. The ion-transport chain of cytochrome oxidase provides an introduction to the molecular mechanisms by which ions are moved across membranes in energy-coupling systems.

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Year:  1980        PMID: 6256734      PMCID: PMC350290          DOI: 10.1073/pnas.77.11.6391

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  14 in total

1.  Resolution of cytochrome oxidase into two component complexes.

Authors:  M Fry; H Vande Zande; D E Green
Journal:  Proc Natl Acad Sci U S A       Date:  1978-12       Impact factor: 11.205

Review 2.  Molecular mechanism of mitochondrial energy coupling.

Authors:  D E Green; G A Blondin
Journal:  Bioscience       Date:  1978-01       Impact factor: 8.589

3.  Studies on the electron transfer system. 68. Formation of membranes as the basis of the reconstitution of the mitochondrial electron transfer system.

Authors:  A Tzagoloff; D H MacLennan; D G McConnell; D E Green
Journal:  J Biol Chem       Date:  1967-05-10       Impact factor: 5.157

Review 4.  Chemiosmotic coupling in oxidative and photosynthetic phosphorylation.

Authors:  P Mitchell
Journal:  Biol Rev Camb Philos Soc       Date:  1966-08

5.  The gramicidin A transmembrane channel: a proposed pi(L,D) helix.

Authors:  D W Urry
Journal:  Proc Natl Acad Sci U S A       Date:  1971-03       Impact factor: 11.205

6.  Investigation of the essential boundary layer phospholipids of cytochrome c oxidase using Triton X-100 delipidation.

Authors:  N C Robinson; F Strey; L Talbert
Journal:  Biochemistry       Date:  1980-08-05       Impact factor: 3.162

7.  Cardiolipin requirement by cytochrome oxidase and the catalytic role of phospholipid.

Authors:  M Fry; D E Green
Journal:  Biochem Biophys Res Commun       Date:  1980-04-29       Impact factor: 3.575

8.  On reagents that convert cytochrome oxidase from an inactive to an active coupling state.

Authors:  D E Green; M Fry
Journal:  Proc Natl Acad Sci U S A       Date:  1980-04       Impact factor: 11.205

9.  Phospholipids as ionophores.

Authors:  C A Tyson; H Vande Zande; D E Green
Journal:  J Biol Chem       Date:  1976-03-10       Impact factor: 5.157

10.  Active calcium treatment transport via coupling between the enzymatic and the ionophoric sites of Ca2+ + Mg2+-ATPase.

Authors:  A E Shamoo; T L Scott; T E Ryan
Journal:  J Supramol Struct       Date:  1977
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  3 in total

1.  A critique of the chemosmotic model of energy coupling.

Authors:  D E Green
Journal:  Proc Natl Acad Sci U S A       Date:  1981-04       Impact factor: 11.205

2.  Universal energy principle of biological systems and the unity of bioenergetics.

Authors:  D E Green; H D Zande
Journal:  Proc Natl Acad Sci U S A       Date:  1981-09       Impact factor: 11.205

3.  The effects of partially hydrogenated marine oils on the mitochondrial function and membrane phospholipid fatty acids in rat heart.

Authors:  R Blomstrand; L Svensson
Journal:  Lipids       Date:  1983-03       Impact factor: 1.880

  3 in total

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