Suppr超能文献

氧化型牛心细胞色素c氧化酶垂直和平行模式电子顺磁共振的角度依赖性

Angular dependences of perpendicular and parallel mode electron paramagnetic resonance of oxidized beef heart cytochrome c oxidase.

作者信息

Hunter D J, Oganesyan V S, Salerno J C, Butler C S, Ingledew W J, Thomson A J

机构信息

School of Biological and Medical Sciences, University of St. Andrews, St. Andrews, Fife KY16 9AL, Scotland.

出版信息

Biophys J. 2000 Jan;78(1):439-50. doi: 10.1016/S0006-3495(00)76606-9.

Abstract

Cytochrome c oxidase catalyzes the reduction of oxygen to water with a concomitant conservation of energy in the form of a transmembrane proton gradient. The enzyme has a catalytic site consisting of a binuclear center of a copper ion and a heme group. The spectroscopic parameters of this center are unusual. The origin of broad electron paramagnetic resonance (EPR) signals in the oxidized state at rather low resonant field, the so-called g' = 12 signal, has been a matter of debate for over 30 years. We have studied the angular dependence of this resonance in both parallel and perpendicular mode X-band EPR in oriented multilayers containing cytochrome c oxidase to resolve the assignment. The "slow" form and compounds formed by the addition of formate and fluoride to the oxidized enzyme display these resonances, which result from transitions between states of an integer-spin multiplet arising from magnetic exchange coupling between the five unpaired electrons of high spin Fe(III) heme a(3) and the single unpaired electron of Cu(B). The first successful simulation of similar signals observed in both perpendicular and parallel mode X-band EPR spectra in frozen aqueous solution of the fluoride compound of the closely related enzyme, quinol oxidase or cytochrome bo(3), has been reported recently (Oganesyan et al., 1998, J. Am. Chem. Soc. 120:4232-4233). This suggested that the exchange interaction between the two metal ions of the binuclear center is very weak (|J| approximately 1 cm(-1)), with the axial zero-field splitting (D approximately 5 cm(-1)) of the high-spin heme dominating the form of the ground state. We show that this model accounts well for the angular dependences of the X-band EPR spectra in both perpendicular and parallel modes of oriented multilayers of cytochrome c oxidase derivatives and that the experimental results are inconsistent with earlier schemes that use exchange coupling parameters of several hundred wavenumbers.

摘要

细胞色素c氧化酶催化氧气还原为水,并同时以跨膜质子梯度的形式保存能量。该酶具有一个催化位点,由一个铜离子和一个血红素基团的双核中心组成。这个中心的光谱参数不同寻常。在相当低的共振场下氧化态中宽电子顺磁共振(EPR)信号的起源,即所谓的g' = 12信号,30多年来一直是一个争论的问题。我们研究了在含有细胞色素c氧化酶的取向多层膜中,这种共振在平行和垂直模式X波段EPR中的角度依赖性,以解决其归属问题。“慢”形式以及通过向氧化酶中添加甲酸盐和氟化物形成的化合物显示出这些共振,它们源于高自旋Fe(III)血红素a(3)的五个未成对电子与Cu(B)的单个未成对电子之间磁交换耦合产生的整数自旋多重态状态之间的跃迁。最近报道了在密切相关的酶喹啉氧化酶或细胞色素bo(3)的氟化物化合物的冷冻水溶液中,在垂直和平行模式X波段EPR光谱中观察到的类似信号的首次成功模拟(奥加内相等人,1998年,《美国化学会志》120:4232 - 4233)。这表明双核中心的两个金属离子之间的交换相互作用非常弱(|J|约为1 cm⁻¹), 高自旋血红素的轴向零场分裂(D约为5 cm⁻¹)主导基态形式。我们表明,该模型很好地解释了细胞色素c氧化酶衍生物取向多层膜在垂直和平行模式下X波段EPR光谱的角度依赖性,并且实验结果与使用几百波数的交换耦合参数的早期方案不一致。

相似文献

本文引用的文献

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验