Orientation of the tetranuclear manganese cluster and tyrosine Z in the O-2-evolving complex of photosystem II: An EPR study of the S2Yz center dot state in oriented acetate-inhibited photosystem II membranes

Inhibitory treatment by acetate, followed by illumination and rapid freezin g, is known to trap the S2YZ. state of the O-2-evolving complex (OEC) in ph otosystem II (PS II). An EPR spectrum of this state exhibits broad split si gnals due to the interaction of the tyrosyl radical, Y-Z(.), with the S = 1 /2 S-2 State of the Mn-4 cluster. We present a novel approach to analyze S2 YZ. spectra of one-dimensionally (I-D) oriented acetate-inhibited PS II mem branes to determine the magnitude and relative orientation of the S2YZ. dip olar vector within the membrane. Although there exists a vast body of EPR d ata on isolated spins in oriented membrane sheets, the present study is the first of its kind on dipolar-coupled electron spin pairs in such systems. We demonstrate the feasibility of the technique and establish a rigorous tr eatment to account for the disorder present in partially oriented 1-D membr ane preparations. We find that (i) the point-dipole distance between Y-Z(.) and the Mn-4 cluster is 7.9 +/- 0.2 Angstrom, (ii) the angle between the i nterspin vector and the thylakoid membrane normal is 75 degrees, (iii) the g(z)-axis of the Mn-4 cluster is 70 degrees away from the membrane normal a nd 35 degrees away from the interspin vector, and (iv) the exchange interac tion between the two spins is -275 x 10(-4) cm(-1), which is antiferromagne tic. Due to the sensitivity of EPR line shapes of oriented spin-coupled pai rs to the interspin distance, the present study imposes a tighter constrain t on the Y-Z-Mn-4 point-dipole distance than obtained from randomly oriente d samples. The geometric constraints obtained from the 1-D oriented sample are combined with published models of the structure of Mn-depleted PS Il to propose a location of the Mn-4 cluster. A structure in which Y-Z is hydrog en bonded to a manganese-bound hydroxide ligand is consistent with availabl e data and favors maximal orbital overlap between the two redox center that would facilitate direct electron- and proton-transfer steps.