化学
电子顺磁共振
领域(数学)
高铁血红蛋白
分析化学(期刊)
零场分裂
材料科学
超精细结构
原子物理学
核磁共振
电子
物理
自旋极化
有机化学
血红蛋白
数学
量子力学
纯数学
作者
Joscha Nehrkorn,Berta M. Martins,K. Holldack,Stefan Stoll,Holger Dobbek,Robert Bittl,Alexander Schnegg
出处
期刊:Molecular Physics
[Taylor & Francis]
日期:2013-07-01
卷期号:111 (18-19): 2696-2707
被引量:39
标识
DOI:10.1080/00268976.2013.809806
摘要
A combined X-band and frequency-domain Fourier-transform THz electron paramagnetic resonance (FD-FT THz-EPR) approach has been employed to determine heme Fe(III) S = 5/2 zero-field splitting (ZFS) parameters of frozen metHb and metMb solutions, both with fluoro and aquo ligands. Frequency-domain EPR measurements have been carried out by an improved synchrotron-based FD-FT THz-EPR spectrometer. ZFS has been determined by field dependence of spin transitions within the mS = ±1/2 manifold, for all four protein systems, and by zero-field spin transitions between mS = ±1/2 and mS = ±3/2 levels, for metHb and metMb flouro-states. FD-FT THz-EPR data were simulated with a novel numerical routine based on Easyspin, which allows now for direct comparison of EPR spectra in field and frequency domain. We found purely axial ZFSs of D = 5.0(1) cm−1 (flouro-metMb), D = 9.2(4) cm−1 (aquo-metMb), D = 5.1(1) cm−1 (flouro-metHB) and D = 10.4(2) cm−1 (aquo-metHb).
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