Function of redox-active tyrosine in photosystem II

52Citations
Citations of this article
63Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

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.

Cite

CITATION STYLE

APA

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

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free