Insights into the protonation state and spin structure for the g=2 multiline electron paramagnetic resonance signal of the oxygen-evolving complex

In photosystem II (PSII), one-electron oxidation of the most stable oxidation state of the Mn4CaO5 cluster (S-1) leads to formation of two distinct states, the open-cubane S-2 conformation [Mn1(III)Mn2(IV)Mn3(IV)Mn4(IV)] with low spin and the closed-cubane S-2 conformation [Mn1(IV)Mn2(IV)Mn3(IV)Mn4(III)] with high spin. In electron paramagnetic resonance (EPR) spectroscopy, the open-cubane S-2 conformation exhibits a g = 2 multiline signal. However, its protonation state remains unclear. Here, we investigated the protonation state of the open-cubane S-2 conformation by calculating exchange couplings in the presence of the PSII protein environment and simulating the pulsed electron-electron double resonance (PELDOR). When a ligand water molecule, which forms an H-bond with D1-Asp61 (W1), is deprotonated at dangling Mn4(IV), the first-exited energy (34 cm(-1)) in manifold spin excited states aligns with the observed value in temperature-dependent pulsed EPR analyses, and the PELDOR signal is best reproduced. Consequently, the g = 2 multiline signal observed in EPR corresponds to the open-cubane S-2 conformation with the deprotonated W1 (OH-).

Automated summary

In photosystem II (PSII), the one-electron oxidation of the Mn4CaO5 cluster leads to the formation of two distinct states, the open-cubane S-2 conformation with low spin and the closed-cubane S-2 conformation with high spin. By calculating exchange couplings in the protein environment and simulating pulsed electron-electron double resonance, the protonation state of the open-cubane S-2 conformation was determined to have a deprotonated water molecule, resulting in the observed g = 2 multiline signal in electron paramagnetic resonance.