Literature DB >> 12609910

The position of QB in the photosynthetic reaction center depends on pH: a theoretical analysis of the proton uptake upon QB reduction.

Antoine Taly1, Pierre Sebban, Jeremy C Smith, G Matthias Ullmann.   

Abstract

Electrostatics-based calculations have been performed to examine the proton uptake upon reduction of the terminal electron acceptor Q(B) in the photosynthetic reaction center of Rhodobacter sphaeroides as a function of pH and the associated conformational equilibrium. Two crystal structures of the reaction center were considered: one structure was determined in the dark and the other under illumination. In the two structures, the Q(B) was found in two different positions, proximal or distal to the nonheme iron. Because Q(B) was found mainly in the distal position in the dark and only in the proximal position under illumination, the two positions have been attributed mostly to the oxidized and the reduced forms of Q(B), respectively. We calculated the proton uptake upon Q(B) reduction by four different models. In the first model, Q(B) is allowed to equilibrate between the two positions with either oxidation state. This equilibrium was allowed to vary with pH. In the other three models the distribution of Q(B) between the proximal position and the distal position was pH-independent, with Q(B) occupying only the distal position or only the proximal position or populating the two positions with a fixed ratio. Only the first model, which includes the pH-dependent conformational equilibrium, reproduces both the experimentally measured pH dependence of the proton uptake and the crystallographically observed conformational equilibrium at pH 8. From this model, we find that Q(B) occupies only the distal position below pH 6.5 and only the proximal position above pH 9.0 in both oxidation states. Between these pH values both positions are partially occupied. The reduced Q(B) has a higher occupancy in the proximal position than the oxidized Q(B). In summary, the present results indicate that the conformational equilibrium of Q(B) depends not only on the redox state of Q(B), but also on the pH value of the solution.

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Year:  2003        PMID: 12609910      PMCID: PMC1302777          DOI: 10.1016/S0006-3495(03)75016-4

Source DB:  PubMed          Journal:  Biophys J        ISSN: 0006-3495            Impact factor:   4.033


  54 in total

1.  pKa's of ionizable groups in proteins: atomic detail from a continuum electrostatic model.

Authors:  D Bashford; M Karplus
Journal:  Biochemistry       Date:  1990-11-06       Impact factor: 3.162

2.  Protonation of interacting residues in a protein by a Monte Carlo method: application to lysozyme and the photosynthetic reaction center of Rhodobacter sphaeroides.

Authors:  P Beroza; D R Fredkin; M Y Okamura; G Feher
Journal:  Proc Natl Acad Sci U S A       Date:  1991-07-01       Impact factor: 11.205

3.  Structure of the membrane-bound protein photosynthetic reaction center from Rhodobacter sphaeroides.

Authors:  C H Chang; O el-Kabbani; D Tiede; J Norris; M Schiffer
Journal:  Biochemistry       Date:  1991-06-04       Impact factor: 3.162

4.  Electrostatic calculations of amino acid titration and electron transfer, Q-AQB-->QAQ-B, in the reaction center.

Authors:  P Beroza; D R Fredkin; M Y Okamura; G Feher
Journal:  Biophys J       Date:  1995-06       Impact factor: 4.033

Review 5.  Electrostatic interactions in macromolecules: theory and applications.

Authors:  K A Sharp; B Honig
Journal:  Annu Rev Biophys Biophys Chem       Date:  1990

6.  Focusing of electric fields in the active site of Cu-Zn superoxide dismutase: effects of ionic strength and amino-acid modification.

Authors:  I Klapper; R Hagstrom; R Fine; K Sharp; B Honig
Journal:  Proteins       Date:  1986-09

7.  Electron acceptors of bacterial photosynthetic reaction centers. II. H+ binding coupled to secondary electron transfer in the quinone acceptor complex.

Authors:  C A Wraight
Journal:  Biochim Biophys Acta       Date:  1979-11-08

8.  Polar hydrogen positions in proteins: empirical energy placement and neutron diffraction comparison.

Authors:  A T Brünger; M Karplus
Journal:  Proteins       Date:  1988

9.  Electrostatic calculations of the pKa values of ionizable groups in bacteriorhodopsin.

Authors:  D Bashford; K Gerwert
Journal:  J Mol Biol       Date:  1992-03-20       Impact factor: 5.469

Review 10.  Nobel lecture. The photosynthetic reaction centre from the purple bacterium Rhodopseudomonas viridis.

Authors:  J Deisenhofer; H Michel
Journal:  EMBO J       Date:  1989-08       Impact factor: 11.598

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  2 in total

Review 1.  Investigating the mechanisms of photosynthetic proteins using continuum electrostatics.

Authors:  G Matthias Ullmann; Edda Kloppmann; Timm Essigke; Eva-Maria Krammer; Astrid R Klingen; Torsten Becker; Elisa Bombarda
Journal:  Photosynth Res       Date:  2008-05-14       Impact factor: 3.573

2.  Time-resolved crystallographic studies of light-induced structural changes in the photosynthetic reaction center.

Authors:  Richard H G Baxter; Nina Ponomarenko; Vukica Srajer; Reinhard Pahl; Keith Moffat; James R Norris
Journal:  Proc Natl Acad Sci U S A       Date:  2004-04-08       Impact factor: 11.205

  2 in total

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