Water oxidation at photosystem II Mn-cluster is mediated by the redox-active tyrosine YZ. We calculated the redox potential (E m) of YZ and its symmetrical counterpart YD, by solving the linearized Poisson-Boltzmann equation. The calculated E m(Y./Y-) were +926 mV/+694 mV for Y Z/YD with the Mn-cluster in S2 state. Together with the asymmetric position of the Mn-cluster relative to YZ/D, differences in H-bond network between YZ (YZ/D1-His 190/D1-Asn298) and YD (YD/D2- His189/D2-Arg294/CP47-Glu364) are crucial for Em(YZ/D). When D1-His190 is protonated, corresponding to a thermally activated state, the calculated E m(YZ) was +1216 mV, which is as high as the Em for PD1/D2. We observed deprotonation at CP43-Arg357 upon S-state transition, which may suggest its involvement in the proton exit pathway. Em(YD) was affected by formation of P D2+ (but not PD1+) and sensitive to the protonation state of D2-Arg180. This points to an electrostatic link between YD and PD2. © 2006 by the Biophysical Society.
CITATION STYLE
Ishikita, H., & Knapp, E. W. (2006). Function of redox-active tyrosine in photosystem II. Biophysical Journal, 90(11), 3886–3896. https://doi.org/10.1529/biophysj.105.076984
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