Investigating the Structure and Dynamics of Apo-Photosystem II

Journal article


Publication Details


Author list: Han R., Rempfer K., Zhang M., Dobbek H., Zouni A., Dau H., Luber S.

Journal: ChemCatChem

Publication year: 2019

Volume number: 11

Issue number: 16

Pages: 4072-4080

Publisher: Wiley-VCH Verlag

ISSN: 1867-3880

eISSN: 1867-3899

DOI: 10.1002/cctc.201900351

URL: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85068175221&origin=inward

Languages: English-Great Britain


Abstract


Photosynthetic water oxidation is a model for future technologies employing solar energy to split water into hydrogen and oxygen. Natural water oxidation is carried out by a special manganese catalyst, the water-oxidizing complex (WOC), located in photosystem II (PSII) of cyanobacteria, algae, and plants. Hence, there is great interest in the molecular structure as well as structural changes during catalytic activity and assembly/disassembly of the WOC. In particular, the light-driven assembly during photosystem II repair under physiological conditions is poorly understood, and structural information about manganese depleted PSII (apo-PSII) is required as a starting point for improving this understanding. Recently Zhang et al. (eLife 2017;6:e26933) showed that the cavity harboring the WOC in PSII remains largely intact upon manganese-depletion and suggested that deprotonation of hydrogen-bonding pairs enables the charge-compensated insertion of the manganese cations without any major change of the cavity structure. By computational methods we have further investigated the structure of apo-PSII and show how it can be stabilized by protons localized at the terminal carboxylate groups inside the remaining cavity. Ab-initio molecular dynamics simulations suggest that not more than two water molecules fill the void left by manganese depletion.



Authors/Editors

Last updated on 2022-28-09 at 19:56