Cryo–electron microscopy reveals hydrogen positions and water networks in photosystem II

Author:

Hussein Rana1ORCID,Graça André23ORCID,Forsman Jack2ORCID,Aydin A. Orkun3ORCID,Hall Michael2ORCID,Gaetcke Julia1ORCID,Chernev Petko3ORCID,Wendler Petra4ORCID,Dobbek Holger1ORCID,Messinger Johannes35ORCID,Zouni Athina1ORCID,Schröder Wolfgang P.25ORCID

Affiliation:

1. Humboldt-Universität zu Berlin, Department of Biology, D 10099 Berlin, Germany.

2. Department of Chemistry, Umeå University, SE 90187 Umeå, Sweden.

3. Molecular Biomimetics, Department of Chemistry- Ångström Laboratory, Uppsala University, SE 75120 Uppsala, Sweden.

4. Institute of Biochemistry and Biology, Department of Biochemistry, University of Potsdam, Karl-Liebknecht Strasse 24-25, D 14476, Potsdam-Golm, Germany.

5. Umeå Plant Science Centre, Department of Plant Physiology, Umeå University, Sweden.

Abstract

Photosystem II starts the photosynthetic electron transport chain that converts solar energy into chemical energy and thus sustains life on Earth. It catalyzes two chemical reactions: water oxidation to molecular oxygen and plastoquinone reduction. Coupling of electron and proton transfer is crucial for efficiency; however, the molecular basis of these processes remains speculative owing to uncertain water binding sites and the lack of experimentally determined hydrogen positions. We thus collected high-resolution cryo–electron microscopy data of fully hydrated photosystem II from the thermophilic cyanobacterium Thermosynechococcus vestitus to a final resolution of 1.71 angstroms. The structure reveals several previously undetected partially occupied water binding sites and more than half of the hydrogen and proton positions. This clarifies the pathways of substrate water binding and plastoquinone B protonation.

Publisher

American Association for the Advancement of Science (AAAS)

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