Literature DB >> 2426249

Organization and function of cytochrome b and ubiquinone in the cristae membrane of beef heart mitochondria.

G von Jagow, T A Link, T Ohnishi.   

Abstract

The arrangement and function of the redox centers of the mammalian bc1 complex is described on the basis of structural data derived from amino acid sequence studies and secondary structure predictions and on the basis of functional studies (i.e., EPR data, inhibitor studies, and kinetic experiments). Two ubiquinone reaction centers do exist--a QH2 oxidation center situated at the outer, cytosolic surface of the cristae membrane (Q0 center), and a Q reduction center (Qi center) situated more to the inner surface of the cristae membrane. The Q0 center is formed by the b-566 domain of cytochrome b, the FeS protein, and maybe an additional small subunit, whereas the Qi center is formed by the b-562 domain of cytochrome b and presumably the 13.4 kDa protein ("QP-C"). The "Q binding proteins" are proposed to be protein subunits of the Q reaction centers of various multiprotein complexes. The path of electron flow branches at the Q0 center, half of the electrons flowing via the high-potential cytochrome chain to oxygen and half of the electrons cycling back into the Q pool via the cytochrome b path connecting the two Q reaction centers. During oxidation of QH2, 2H+ are released to the cytosolic space and during reduction of Q, 2H+ are taken up from the matrix side, resulting in a net transport across the membrane of 2H+ per e- flown from QH2 to cytochrome c, the H+ being transported across the membrane as H (H+ + e-) by the mobile carrier Q. The authors correct their earlier view of cytochrome b functioning as a H+ pump, proposing that the redox-linked pK changes of the acidic groups of cytochrome b are involved in the protonation/deprotonation processes taking place during the reduction and oxidation of Q. The reviewers stress that cytochrome b is in equilibrium with the Q pool via the Qi center, but not via the Q0 center. Their view of the mechanisms taking place at the reductase is a Q cycle linked to a Q-pool where cytochrome b is acting as an electron pump.

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Year:  1986        PMID: 2426249     DOI: 10.1007/bf00743462

Source DB:  PubMed          Journal:  J Bioenerg Biomembr        ISSN: 0145-479X            Impact factor:   2.945


  42 in total

1.  Purification of a reconstitutively active iron-sulfur protein (oxidation factor) from succinate . cytochrome c reductase complex of bovine heart mitochondria.

Authors:  B L Trumpower; C A Edwards
Journal:  J Biol Chem       Date:  1979-09-10       Impact factor: 5.157

2.  Protonmotive redox mechanism of the cytochrome b-c1 complex in the respiratory chain: protonmotive ubiquinone cycle.

Authors:  P Mitchell
Journal:  FEBS Lett       Date:  1975-08-01       Impact factor: 4.124

3.  The chromone inhibitor stigmatellin--binding to the ubiquinol oxidation center at the C-side of the mitochondrial membrane.

Authors:  G von Jagow; T Ohnishi
Journal:  FEBS Lett       Date:  1985-06-17       Impact factor: 4.124

4.  The kinetics of the redox reactions of ubiquinone related to the electron-transport activity in the respiratory chain.

Authors:  A Kröger; M Klingenberg
Journal:  Eur J Biochem       Date:  1973-04

Review 5.  The mechanism of action of the respiratory inhibitor, antimycin.

Authors:  E C Slater
Journal:  Biochim Biophys Acta       Date:  1973-12-07

6.  The properties of the mitochondrial succinate-cytochrome c reductase.

Authors:  D F Wilson; M Erecińska; J S Leigh; M Koppelman
Journal:  Arch Biochem Biophys       Date:  1972-07       Impact factor: 4.013

7.  Oudemansin, strobilurin A, strobilurin B and myxothiazol: new inhibitors of the bc1 segment of the respiratory chain with an E-beta-methoxyacrylate system as common structural element.

Authors:  W F Becker; G von Jagow; T Anke; W Steglich
Journal:  FEBS Lett       Date:  1981-09-28       Impact factor: 4.124

8.  The pathway of electrons through OH2:cytochrome c oxidoreductase studied by pre-steady -state kinetics.

Authors:  S De Vries; S P Albracht; J A Berden; E C Slater
Journal:  Biochim Biophys Acta       Date:  1982-07-22

9.  A model for the cytochrome b dimer of the ubiquinol: cytochrome c oxidoreductase as a proton translocator.

Authors:  G von Jagow; W D Engel
Journal:  FEBS Lett       Date:  1980-02-25       Impact factor: 4.124

10.  Sequence homology and structural similarity between cytochrome b of mitochondrial complex III and the chloroplast b6-f complex: position of the cytochrome b hemes in the membrane.

Authors:  W R Widger; W A Cramer; R G Herrmann; A Trebst
Journal:  Proc Natl Acad Sci U S A       Date:  1984-02       Impact factor: 11.205

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  5 in total

1.  Evolutionary conservation of protein regions in the protonmotive cytochrome b and their possible roles in redox catalysis.

Authors:  N Howell
Journal:  J Mol Evol       Date:  1989-08       Impact factor: 2.395

Review 2.  Phorphorylative electron transport chains lacking a cytochrome bc1 complex.

Authors:  A Kröger; J Paulsen; I Schröder
Journal:  J Bioenerg Biomembr       Date:  1986-06       Impact factor: 2.945

3.  The genes for cytochrome b, ND 4L, ND6 and two tRNAs from the mitochondrial genome of the locust, Locusta migratoria.

Authors:  R M Rippe; G Gellissen
Journal:  Curr Genet       Date:  1994-02       Impact factor: 3.886

Review 4.  What information do inhibitors provide about the structure of the hydroquinone oxidation site of ubihydroquinone: cytochrome c oxidoreductase?

Authors:  T A Link; U Haase; U Brandt; G von Jagow
Journal:  J Bioenerg Biomembr       Date:  1993-06       Impact factor: 2.945

5.  Cellular quantitative structure-activity relationship (Cell-QSAR): conceptual dissection of receptor binding and intracellular disposition in antifilarial activities of Selwood antimycins.

Authors:  Senthil Natesan; Tiansheng Wang; Viera Lukacova; Vladimir Bartus; Akash Khandelwal; Rajesh Subramaniam; Stefan Balaz
Journal:  J Med Chem       Date:  2012-04-11       Impact factor: 7.446

  5 in total

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