In vitro oligomerization of a membrane protein complex -: Liposome-based reconstitution of trimeric photosystem I from isolated monomers

被引:59
作者
Kruip, J
Karapetyan, NV
Terekhova, IV
Rögner, M
机构
[1] Ruhr Univ Bochum, Fac Biol, D-44780 Bochum, Germany
[2] Russian Acad Sci, AN Bakh Biochem Inst, Moscow 117071, Russia
关键词
D O I
10.1074/jbc.274.26.18181
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
Many membrane proteins can be isolated in different oligomeric forms. Photosystem I (PSI), for example, exists in cyanobacteria either as a monomeric or as a trimeric complex. Neither the factors responsible for the specific trimerization process nor its biological role are known at present. In the filamentous cyanobacterium Spirulina platensis, trimers in contrast to monomers show chlorophyll fluorescence emission at 760 nm. To investigate the oligomerization process as well as the nature of the long wavelength chlorophylls, we describe here an in vitro reconstitution procedure to assemble trimeric PS I from isolated purified PS I monomers. Monomers (and trimers) were extracted from S. platensis with n-dodecyl p-D-maltoside and further purified by perfusion chromatography steps. The isolated complexes had the same polypeptide composition as other cyanobacteria (PsaA-PsaF and PsaI-PsaM), as determined from high resolution gels and immunoblotting. They were incorporated into proteoliposomes, which had been prepared by the detergent absorption method, starting from a phosphatidylcholine:phosphatidic acid mixture solubilized by octylglucoside. After the addition of monomeric PSI (lipid:chlorophyll, 25:1), octylglucoside was gradually removed by the stepwise addition of Biobeads. The 77 K fluorescence emission spectrum of these proteoliposomes displays a long wavelength emission at 760 nm that is characteristic of PS I trimers, which indicates for the first time the successful in vitro reconstitution of PS I trimers, In addition, a high performance liquid chromatography analysis of complexes extracted from these proteoliposomes confirms the formation of structural trimers, We also could show with this system 1) that at least one of the stromal subunits PsaC, -D, and -E is necessary for trimer formation and 2) that the extreme long wavelength emitting chlorophyll is formed as a result of trimer formation.
引用
收藏
页码:18181 / 18188
页数:8
相关论文
共 43 条
[1]  
[Anonymous], 1989, PLANT BIOL
[2]   EVIDENCE FOR A TRIMERIC ORGANIZATION OF THE PHOTOSYSTEM-I COMPLEX FROM THE THERMOPHILIC CYANOBACTERIUM SYNECHOCOCCUS SP [J].
BOEKEMA, EJ ;
DEKKER, JP ;
VANHEEL, MG ;
ROGNER, M ;
SAENGER, W ;
WITT, I ;
WITT, HT .
FEBS LETTERS, 1987, 217 (02) :283-286
[3]   INTRAMEMBRANE HELIX-HELIX ASSOCIATION IN OLIGOMERIZATION AND TRANSMEMBRANE SIGNALING [J].
BORMANN, BJ ;
ENGELMAN, DM .
ANNUAL REVIEW OF BIOPHYSICS AND BIOMOLECULAR STRUCTURE, 1992, 21 :223-242
[4]   FUNCTION AND ORGANIZATION OF PHOTOSYSTEM-I POLYPEPTIDES [J].
CHITNIS, PR ;
XU, Q ;
CHITNIS, VP ;
NECHUSHTAI, R .
PHOTOSYNTHESIS RESEARCH, 1995, 44 (1-2) :23-40
[5]   PSAL SUBUNIT IS REQUIRED FOR THE FORMATION OF PHOTOSYSTEM-I TRIMERS IN THE CYANOBACTERIUM SYNECHOCYSTIS SP PCC-6803 [J].
CHITNIS, VP ;
CHITNIS, PR .
FEBS LETTERS, 1993, 336 (02) :330-334
[6]   Functional reconstitution of photosystem I reaction center from cyanobacterium Synechocystis sp PCC6803 into liposomes using a new reconstitution procedure [J].
Cladera, J ;
Rigaud, JL ;
Bottin, H ;
Dunach, M .
JOURNAL OF BIOENERGETICS AND BIOMEMBRANES, 1996, 28 (06) :503-515
[7]  
Dorra D, 1998, PHOTOSYNTHESIS: MECHANISMS AND EFFECTS, VOLS I-V, P587
[8]   INVESTIGATION OF THE STRUCTURE OF TRIMERIC AND MONOMERIC PHOTOSYSTEM-I REACTION CENTER COMPLEXES [J].
FORD, RC ;
HOLZENBURG, A .
EMBO JOURNAL, 1988, 7 (08) :2287-2293
[9]   ELECTRON-MICROSCOPY OF CYTOCHROME-C-OXIDASE CRYSTALS - MONOMER-DIMER RELATIONSHIP AND CYTOCHROME-C BINDING-SITE [J].
FREY, TG ;
MURRAY, JM .
JOURNAL OF MOLECULAR BIOLOGY, 1994, 237 (03) :275-297
[10]   Structure of photosystem I at 4.5 angstrom resolution: A short review including evolutionary aspects [J].
Fromme, P ;
Witt, HT ;
Schubert, WD ;
Klukas, O ;
Saenger, W ;
Krauss, N .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS, 1996, 1275 (1-2) :76-83