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pH‐Dependent Protonation of Surface Carboxylate Groups in PsbO Enables Local Buffering and Triggers Structural Changes

Photosystem II (PSII) catalyzes the splitting of water, releasing protons and dioxygen. Its highly conserved subunit PsbO extends from the oxygen‐evolving center (OEC) into the thylakoid lumen and stabilizes the catalytic Mn(4)CaO(5) cluster. The high degree of conservation of accessible negatively...

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Detalles Bibliográficos
Autores principales: Gerland, Lisa, Friedrich, Daniel, Hopf, Linus, Donovan, Eavan J., Wallmann, Arndt, Erdmann, Natalja, Diehl, Anne, Bommer, Martin, Buzar, Krzysztof, Ibrahim, Mohamed, Schmieder, Peter, Dobbek, Holger, Zouni, Athina, Bondar, Ana‐Nicoleta, Dau, Holger, Oschkinat, Hartmut
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7318136/
https://www.ncbi.nlm.nih.gov/pubmed/31930693
http://dx.doi.org/10.1002/cbic.201900739
Descripción
Sumario:Photosystem II (PSII) catalyzes the splitting of water, releasing protons and dioxygen. Its highly conserved subunit PsbO extends from the oxygen‐evolving center (OEC) into the thylakoid lumen and stabilizes the catalytic Mn(4)CaO(5) cluster. The high degree of conservation of accessible negatively charged surface residues in PsbO suggests additional functions, as local pH buffer or by affecting the flow of protons. For this discussion, we provide an experimental basis, through the determination of pK (a) values of water‐accessible aspartate and glutamate side‐chain carboxylate groups by means of NMR. Their distribution is strikingly uneven, with high pK (a) values around 4.9 clustered on the luminal PsbO side and values below 3.5 on the side facing PSII. pH‐dependent changes in backbone chemical shifts in the area of the lumen‐exposed loops are observed, indicating conformational changes. In conclusion, we present a site‐specific analysis of carboxylate group proton affinities in PsbO, providing a basis for further understanding of proton transport in photosynthesis.