Kushkuley B, Stavrov S S
Sackler Institute of Molecular Medicine, Sackler School of Medicine, Tel Aviv University, Ramat Aviv, Israel.
Biochim Biophys Acta. 1997 Sep 5;1341(2):238-50. doi: 10.1016/s0167-4838(97)00082-4.
The vibronic theory of chemical activation and quantum chemical calculations are applied to calculate the stretching vibrational frequency of cyanide, coordinated by the complex of ferric porphyrin with imidazole. The results show that the frequency of the stretching vibration of the cyanide strongly depends on its coordination geometry and is hardly affected by the electrostatic perturbations of reasonable magnitude. The comparison of these results with the experimental data on the cyanide complexes of different heme proteins and their models allows to elucidate the cyanide coordination geometry. The combined infrared and resonance Raman scattering experimental investigation of the cyanide and carbonyl complexes with the same heme protein is proposed to distinguish between the steric and electrostatic contributions to the heme-protein interaction.
将化学活化的振动理论和量子化学计算应用于计算由铁卟啉与咪唑形成的配合物所配位的氰化物的伸缩振动频率。结果表明,氰化物伸缩振动的频率强烈依赖于其配位几何结构,并且几乎不受合理大小的静电扰动的影响。将这些结果与不同血红素蛋白及其模型的氰化物配合物的实验数据进行比较,有助于阐明氰化物的配位几何结构。建议对与同一血红素蛋白形成的氰化物和羰基配合物进行红外和共振拉曼散射联合实验研究,以区分空间和静电对血红素-蛋白相互作用的贡献。