Yu N T, Thompson H M, Chang C K
Biophys J. 1987 Feb;51(2):283-7. doi: 10.1016/S0006-3495(87)83334-9.
Resonance Raman spectroscopy has been employed to probe the effects of proximal base strain on the bonding of O2 and CO in three synthetic hemins with covalently linked imidazole ligands. The strain is introduced by varying the length of the imidazole-containing side chain and by restricting the side chain flexibility with a phenyl ring. These hemins are abbreviated as "long," "short," and "stiff" hemins, respectively. In the deoxy state, the iron-imidazole stretching frequencies [nu(Fe--N epsilon)] for long, short, and stiff hemins are detected at 200, 207, and 204 cm-1, respectively. The strain induced in the iron-imidazole bond by the short hemin results in a higher nu(Fe--N epsilon) frequency, in contrast to the strain induced by sterically hindered 2-methylimidazole or 1,2-dimethylimidazole complexes in which the Fe--N epsilon bond is tilted and lengthened, but the imidazole ring remains perpendicular to the heme plane. However, in the short hemin, the plane of the imidazole ring may not be perpendicular to the plane of the porphyrin, altering the amount of pi-interaction (hence the strength of Fe--N epsilon bond) and the nature of normal mode containing Fe--N epsilon bond stretching. Upon CO binding, we have observed the nu(Fe--CO) stretching frequencies at 497 (long), 499 (short), and 496 cm-1 (stiff), somewhat lower than those reported by Mitchell et al. (Inorg. Chem., 1985, 24:967) for the chelated-heme X CO complexes (i.e., 501-506 cm-1). This is the first report of an iron-oxygen-associated vibration observed in solution for an unprotected heme. The oxy complexes were formed by introducing dioxygen to the deoxy complexes at -700C. The isotope-sensitive line was detected at 576 cm- (1602) in oxy stiff hemin, which was shifted to 545 cm-1 upon 1802 substitution. This is perhaps the largest isotope shift (31 cm-') observed to date, compared with the usual 22-24 cm-'.For the long and short hemins, the iron-oxygen-associated vibration was detected at 574 and 573 cm-', respectively.These values are very similar to those observed(N-methylimidazole) and myoglobin/hemoglobin.
共振拉曼光谱已被用于探究在三种带有共价连接咪唑配体的合成血红素中,近端碱基应变对O₂和CO键合的影响。通过改变含咪唑侧链的长度以及用苯环限制侧链的灵活性来引入应变。这些血红素分别简称为“长”、“短”和“硬”血红素。在脱氧状态下,长、短和硬血红素的铁-咪唑伸缩频率[ν(Fe--Nε)]分别在200、207和204cm⁻¹处被检测到。短血红素在铁-咪唑键中诱导产生的应变导致ν(Fe--Nε)频率更高,这与空间位阻的2-甲基咪唑或1,2-二甲基咪唑配合物诱导的应变形成对比,在后者中Fe--Nε键倾斜且变长,但咪唑环仍垂直于血红素平面。然而,在短血红素中,咪唑环的平面可能不垂直于卟啉平面,从而改变了π相互作用的量(进而改变了Fe--Nε键的强度)以及包含Fe--Nε键伸缩的简正模式的性质。在CO结合后,我们观察到ν(Fe--CO)伸缩频率在497(长)、499(短)和496cm⁻¹(硬)处,略低于Mitchell等人(《无机化学》,1985年,24:967)报道的螯合血红素X CO配合物的频率(即501 - 506cm⁻¹)。这是关于未保护血红素在溶液中观察到的铁-氧相关振动的首次报道。通过在-70℃向脱氧配合物中引入双原子氧形成氧配合物。在硬血红素氧配合物中,同位素敏感线在576cm⁻¹(¹⁶O₂)处被检测到,在¹⁸O₂取代后移至545cm⁻¹。与通常的22 - 24cm⁻¹相比,这可能是迄今为止观察到的最大同位素位移(31cm⁻¹)。对于长和短血红素,铁-氧相关振动分别在574和573cm⁻¹处被检测到。这些值与在(N-甲基咪唑)以及肌红蛋白/血红蛋白中观察到的值非常相似。