Cyanobacterial photosystem II at 2.9-Å resolution and the role of quinones, lipids, channels and chloride

被引:950
作者
Guskov, Albert [2 ]
Kern, Jan [1 ]
Gabdulkhakov, Azat [2 ]
Broser, Matthias [1 ]
Zouni, Athina [1 ]
Saenger, Wolfram [2 ]
机构
[1] Tech Univ Berlin, Inst Chem, Max Volmer Lab Biophys Chem, D-10623 Berlin, Germany
[2] Free Univ Berlin, Inst Chem & Biochem Kristallog, D-14195 Berlin, Germany
关键词
CRYSTAL-STRUCTURE; THERMOSYNECHOCOCCUS-ELONGATUS; BINDING-SITE; CYTOCHROME BC(1); WATER OXIDATION; MN4CA COMPLEX; PROTEIN; CALCIUM; PHOSPHATIDYLGLYCEROL; CRYSTALLOGRAPHY;
D O I
10.1038/nsmb.1559
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
Photosystem II ( PSII) is a large homodimeric protein-cofactor complex located in the photosynthetic thylakoid membrane that acts as light-driven water: plastoquinone oxidoreductase. The crystal structure of PSII from Thermosynechococcus elongatus at 2.9-angstrom resolution allowed the unambiguous assignment of all 20 protein subunits and complete modeling of all 35 chlorophyll a molecules and 12 carotenoid molecules, 25 integral lipids and 1 chloride ion per monomer. The presence of a third plastoquinone QC and a second plastoquinone-transfer channel, which were not observed before, suggests mechanisms for plastoquinol-plastoquinone exchange, and we calculated other possible water or dioxygen and proton channels. Putative oxygen positions obtained from a Xenon derivative indicate a role for lipids in oxygen diffusion to the cytoplasmic side of PSII. The chloride position suggests a role in proton-transfer reactions because it is bound through a putative water molecule to the Mn4Ca cluster at a distance of 6.5 angstrom and is close to two possible proton channels. (c) 2009 Nature America, Inc. All rights reserved.
引用
收藏
页码:334 / 342
页数:9
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