On the spatial organization of hemes and chlorophyll in cytochrome b6 f -: A linear and circular dichroism study

被引:22
作者
Schoepp, B
Chabaud, E
Breyton, C
Verméglio, A
Popot, JL
机构
[1] CNRS, Lab Bioenerget & Ingn Prot, F-13402 Marseille 20, France
[2] CNRS UPR 9052, Lab Physicochim Mol Membranes Biol, F-75005 Paris, France
[3] Univ Paris 07, Inst Biol Physicochim, F-75005 Paris, France
[4] CEA, DSV, DEVM, Lab Bioenerget Cellulaire, F-13108 St Paul Les Durance, France
关键词
D O I
10.1074/jbc.275.8.5275
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The organization of chromophores in the cytochrome b(6)f from Chlamydomonas reinhardtii has been studied spectroscopically. Linear dichroism (LD) measurements, performed on the complex co-reconstituted into vesicles with photosynthetic reaction centers as an internal standard, allow the determination of the orientations of the chromophore with respect to the membrane plane. The orientations of the b(H)- and b(L)-hemes are comparable to those determined crystallographically on the cytochrome bc(1). The excitonic CD signal, resulting from the interaction between b-hemes, is similar to that reported for the cytochrome bc(1). LD and CD data are consistent with the differences between the b(6)f and bc(1) leaving the orientation of the b-hemes unaffected. By contrast, the LD data yield a different orientation for the heme f as compared either to the heme c(1) in the crystallographic structures or to the heme fas studied by electron paramagnetic resonance. This difference could either result from incorrect assumptions regarding the orientations of the electronic transitions of the f-heme or may point to the possibility of a redox-dependent movement of cytochrome f. The chlorophyll a was observed in a well defined orientation, further corroborating a specific binding site for it in the b(6)f complex.
引用
收藏
页码:5275 / 5283
页数:9
相关论文
共 68 条
[1]  
Adar F, 1978, PORPHYRINS A, V3, P167
[2]   STRUCTURE OF THE REACTION CENTER FROM RHODOBACTER-SPHAEROIDES R-26 - THE PROTEIN SUBUNITS [J].
ALLEN, JP ;
FEHER, G ;
YEATES, TO ;
KOMIYA, H ;
REES, DC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (17) :6162-6166
[3]   LARGE-SCALE PURIFICATION AND CHARACTERIZATION OF A HIGHLY-ACTIVE 4-SUBUNIT CYTOCHROME BC1 COMPLEX FROM RHODOBACTER-SPHAEROIDES [J].
ANDREWS, KM ;
CROFTS, AR ;
GENNIS, RB .
BIOCHEMISTRY, 1990, 29 (11) :2645-2651
[4]   THE CCP4 SUITE - PROGRAMS FOR PROTEIN CRYSTALLOGRAPHY [J].
BAILEY, S .
ACTA CRYSTALLOGRAPHICA SECTION D-BIOLOGICAL CRYSTALLOGRAPHY, 1994, 50 :760-763
[5]  
Bald D., 1992, RES PHOTOSYNTHESIS, VI, P629
[6]   ELECTRON-PARAMAGNETIC-RES SIGNALS AND ORIENTATION OF CYTOCHROMES IN THE SPINACH CHLOROPLAST THYLAKOID MEMBRANE [J].
BERGSTROM, J ;
VANNGARD, T .
BIOCHIMICA ET BIOPHYSICA ACTA, 1982, 682 (03) :452-456
[7]  
Breton J, 1982, PHOTOSYNTHESIS, P153
[8]  
BRETON J, 1977, THESIS U PARIS 11 OR
[9]  
BRETON J, 1984, ADV PHOTOSYNTHETIC R, P11
[10]   Dimer to monomer conversion of the cytochrome b(6)f complex - Causes and consequences [J].
Breyton, C ;
Tribet, C ;
Olive, J ;
Dubacq, JP ;
Popot, JL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (35) :21892-21900