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Structure of cyanobacterial photosystem I complexed with ferredoxin at 1.97 Å resolution.
Li, Jiannan; Hamaoka, Noriyuki; Makino, Fumiaki; Kawamoto, Akihiro; Lin, Yuxi; Rögner, Matthias; Nowaczyk, Marc M; Lee, Young-Ho; Namba, Keiichi; Gerle, Christoph; Kurisu, Genji.
Afiliación
  • Li J; Laboratory for Protein Crystallography, Institute for Protein Research, Osaka University, Suita, Osaka, 565-0871, Japan.
  • Hamaoka N; Department of Biological Sciences, Graduate School of Science, Osaka University, Toyonaka, Osaka, 560-0043, Japan.
  • Makino F; Laboratory for Protein Crystallography, Institute for Protein Research, Osaka University, Suita, Osaka, 565-0871, Japan.
  • Kawamoto A; Department of Macromolecular Science, Graduate School of Science, Osaka University, Toyonaka, Osaka, 560-0043, Japan.
  • Lin Y; Graduate School of Frontier Biosciences, Osaka University, Suita, Osaka, 565-0871, Japan.
  • Rögner M; JEOL Ltd., Akishima, Tokyo, Japan.
  • Nowaczyk MM; Laboratory for Protein Crystallography, Institute for Protein Research, Osaka University, Suita, Osaka, 565-0871, Japan.
  • Lee YH; Research Center for Bioconvergence Analysis, Korea Basic Science Institute, Ochang, Chungbuk, 28119, South Korea.
  • Namba K; Plant Biochemistry, Faculty of Biology and Biotechnology, Ruhr University Bochum, 44780, Bochum, Germany.
  • Gerle C; Plant Biochemistry, Faculty of Biology and Biotechnology, Ruhr University Bochum, 44780, Bochum, Germany.
  • Kurisu G; Research Center for Bioconvergence Analysis, Korea Basic Science Institute, Ochang, Chungbuk, 28119, South Korea.
Commun Biol ; 5(1): 951, 2022 09 12.
Article en En | MEDLINE | ID: mdl-36097054
Photosystem I (PSI) is a light driven electron pump transferring electrons from Cytochrome c6 (Cyt c6) to Ferredoxin (Fd). An understanding of this electron transfer process is hampered by a paucity of structural detail concerning PSI:Fd interface and the possible binding sites of Cyt c6. Here we describe the high resolution cryo-EM structure of Thermosynechococcus elongatus BP-1 PSI in complex with Fd and a loosely bound Cyt c6. Side chain interactions at the PSI:Fd interface including bridging water molecules are visualized in detail. The structure explains the properties of mutants of PsaE and PsaC that affect kinetics of Fd binding and suggests a molecular switch for the dissociation of Fd upon reduction. Calorimetry-based thermodynamic analyses confirms a single binding site for Fd and demonstrates that PSI:Fd complexation is purely driven by entropy. A possible reaction cycle for the efficient transfer of electrons from Cyt c6 to Fd via PSI is proposed.
Asunto(s)

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Cianobacterias / Complejo de Proteína del Fotosistema I Idioma: En Revista: Commun Biol Año: 2022 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Cianobacterias / Complejo de Proteína del Fotosistema I Idioma: En Revista: Commun Biol Año: 2022 Tipo del documento: Article