Analysis of dipolar and exchange interactions between manganese and tyrosine Z in the S2YZ• state of acetate-inhibited photosystem II via EPR spectral simulations at X- and Q-Bands

被引:84
作者
Lakshmi, KV
Eaton, SS
Eaton, GR
Frank, HA
Brudvig, GW
机构
[1] Yale Univ, Dept Chem, New Haven, CT 06520 USA
[2] Univ Denver, Dept Chem & Biochem, Denver, CO 80208 USA
[3] Univ Connecticut, Dept Chem, Storrs, CT 06269 USA
来源
JOURNAL OF PHYSICAL CHEMISTRY B | 1998年 / 102卷 / 42期
关键词
D O I
10.1021/jp982140p
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Upon room-temperature illumination, acetate-inhibited photosystem II membranes are known to exhibit a 240 G wide X-band (similar to 9.5 GHz) electron paramagnetic resonance (EPR) signal at 10 K. This EPR signal arises from an interaction between the S = 1/2 multiline S-2 state of the tetranuclear manganese cluster and an oxidized tyrosine residue, Y-Z(.). In the present study, the exchange and dipolar interactions between the two paramagnetic species are simulated at X- and Q-band (similar to 33 GHz) frequencies utilizing second-order perturbation theory. The positions and relative intensities of the hyperfine lines in the S = 1/2 S-2 state multiline EPR signal of the noninteracting Mn-4 cluster are accurately simulated by including g anisotropy and four sets of axially symmetric Mn-55 hyperfine tensors. These parameters are then used to simulate the dipolar and exchange interactions giving rise to the interacting S2YZ. (formerly referred to as S3) EPR signal. Relative intensities of components of the S2YZ. EPR spectrum, at both X- and Q-band frequencies, are best reproduced with a dipolar coupling corresponding to an interspin distance of 7.7 Angstrom and an exchange coupling (J) of -280 x 10(-4) cm(-1).
引用
收藏
页码:8327 / 8335
页数:9
相关论文
共 38 条
[1]   Pulsed EPR study of the S'(3) signal in the Ca2+-depleted photosystem II [J].
Astashkin, AV ;
MIno, H ;
Kawamori, A ;
Ono, TA .
CHEMICAL PHYSICS LETTERS, 1997, 272 (5-6) :506-516
[2]   MECHANISM OF PHOTOINHIBITION OF PHOTOSYNTHETIC WATER OXIDATION BY CL- DEPLETION AND F- SUBSTITUTION - OXIDATION OF A PROTEIN RESIDUE [J].
BAUMGARTEN, M ;
PHILO, JS ;
DISMUKES, GC .
BIOCHEMISTRY, 1990, 29 (48) :10814-10822
[3]   ACTIVE AND RESTING STATES OF THE O-12-EVOLVING COMPLEX OF PHOTOSYSTEM-II [J].
BECK, WF ;
DEPAULA, JC ;
BRUDVIG, GW .
BIOCHEMISTRY, 1985, 24 (12) :3035-3043
[4]   A HIGHLY RESOLVED, OXYGEN-EVOLVING PHOTOSYSTEM-II PREPARATION FROM SPINACH THYLAKOID MEMBRANES - ELECTRON-PARAMAGNETIC-RES AND ELECTRON-TRANSPORT PROPERTIES [J].
BERTHOLD, DA ;
BABCOCK, GT ;
YOCUM, CF .
FEBS LETTERS, 1981, 134 (02) :231-234
[5]   THEORETICAL-STUDY OF THE MULTILINE EPR SIGNAL FROM THE S2 STATE OF THE OXYGEN EVOLVING COMPLEX OF PHOTOSYSTEM-II - EVIDENCE FOR A MAGNETIC TETRAMER [J].
BONVOISIN, J ;
BLONDIN, G ;
GIRERD, JJ ;
ZIMMERMANN, JL .
BIOPHYSICAL JOURNAL, 1992, 61 (05) :1076-1086
[6]   NATURE OF THE INHIBITION OF THE OXYGEN-EVOLVING ENZYME OF PHOTOSYSTEM-II INDUCED BY NACL WASHING AND REVERSED BY THE ADDITION OF CA-2+ OR SR-2+ [J].
BOUSSAC, A ;
RUTHERFORD, AW .
BIOCHEMISTRY, 1988, 27 (09) :3476-3483
[7]   LIMIT FUNCTION FOR LONG-RANGE FERROMAGNETIC AND ANTI-FERROMAGNETIC SUPEREXCHANGE [J].
COFFMAN, RE ;
BUETTNER, GR .
JOURNAL OF PHYSICAL CHEMISTRY, 1979, 83 (18) :2387-2392
[8]   THE MANGANESE AND CALCIUM-IONS OF PHOTOSYNTHETIC OXYGEN EVOLUTION [J].
DEBUS, RJ .
BIOCHIMICA ET BIOPHYSICA ACTA, 1992, 1102 (03) :269-352
[9]  
DORLET P, IN PRESS J PHYS CHEM
[10]  
Eaton G.R., 1989, SPIN LABELING THEORY, P339