Distinct structural modulation of photosystem I and lipid environment stabilizes its tetrameric assembly

被引:32
作者
Chen, Ming [1 ,2 ]
Perez-Boerema, Annemarie [2 ,3 ]
Zhang, Laixing [4 ]
Li, Yanxue [1 ]
Yang, Maojun [4 ]
Li, Shizhong [1 ]
Amunts, Alexey [2 ,3 ]
机构
[1] Tsinghua Univ, Beijing Engn Res Ctr Biofuels, Inst Nucl & New, Beijing, Peoples R China
[2] Stockholm Univ, Dept Biochem & Biophys, Sci Life Lab, Solna, Sweden
[3] Karolinska Inst, Dept Med Biochem & Biophys, Stockholm, Sweden
[4] Tsinghua Univ, Beijing Adv Innovat Ctr Struct Biol, Sch Life Sci, Minist Educ,Key Lab Prot Sci,Tsinghua Peking Join, Beijing, Peoples R China
基金
欧盟地平线“2020”; 欧洲研究理事会; 中国国家自然科学基金;
关键词
CRYO-EM STRUCTURE; CYANOBACTERIAL; SUPERCOMPLEX; COMPLEX; LIGHT; ORGANIZATION; VISUALIZATION; VALIDATION; ANABAENA;
D O I
10.1038/s41477-020-0610-x
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Photosystem I (PSI) is able to form different oligomeric states across various species. To reveal the structural basis for PSI dimerization and tetramerization, we structurally investigated PSI from the cyanobacterium Anabaena. This revealed a disrupted trimerization domain due to lack of the terminal residues of PsaL in the lumen, which resulted in PSI dimers with loose connections between monomers and weaker energy-coupled chlorophylls than in the trimer. At the dimer surface, specific phospholipids, cofactors and interactions in combination facilitated recruitment of another dimer to form a tetramer. Taken together, the relaxed luminal connections and lipid specificity at the dimer interface account for membrane curvature. PSI tetramer assembly appears to increase the surface area of the thylakoid membrane, which would contribute to PSI crowding. Photosystem I from the cyanobacterium Anabaena has a disrupted trimerization domain resulting in dimers with loose connections between monomers. Phospholipids and cofactors at the dimer surface facilitate further dimerization to form a tetramer.
引用
收藏
页码:314 / +
页数:17
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