Kroes S J, Hoitink C W, Andrew C R, Ai J, Sanders-Loehr J, Messerschmidt A, Hagen W R, Canters G W
Leiden Institute of Chemistry, Gorlaeus Laboratories, Leiden University, The Netherlands.
Eur J Biochem. 1996 Sep 1;240(2):342-51. doi: 10.1111/j.1432-1033.1996.0342h.x.
The Cu ligand Met121 in azurin of Alcaligenes denitrificans was mutated to His. The spectroscopic and mechanistic properties of [M121H]azurin appear to be pH dependent with a pKa of 3.8 due to the ionization of His121. The [M121H]azurin mutant exhibits two major distinct metal-site-coordination geometries which coexist in solution according to pH-dependent equilibrium. Both species have been spectroscopically characterized by ultraviolet-visible, EPR and resonance Raman spectroscopies. At neutral pH, His121 is deprotonated and acts as the fourth ligand of the Cu; the spectroscopic characteristics of the Cu site at this pH are halfway between those of a type-1 and a type-2 Cu site, and the site is referred to as a type-1.5 or intermediate Cu site. The spectral data are compatible with a tetrahedral geometry of this site. At low pH, the spectroscopic data indicate that [M121H]azurin has a trigonal type-1 rhombic Cu site.
将反硝化产碱菌天青蛋白中的铜配体甲硫氨酸121突变为组氨酸。由于组氨酸121的电离作用,[M121H]天青蛋白的光谱和机理性质似乎依赖于pH值,其pKa为3.8。[M121H]天青蛋白突变体表现出两种主要的、不同的金属位点配位几何结构,它们根据pH依赖的平衡共存于溶液中。这两种物种都已通过紫外可见光谱、电子顺磁共振光谱和共振拉曼光谱进行了光谱表征。在中性pH值下,组氨酸121去质子化并作为铜的第四个配体;该pH值下铜位点的光谱特征介于1型和2型铜位点之间,该位点被称为1.5型或中间铜位点。光谱数据与该位点的四面体几何结构相符。在低pH值下,光谱数据表明[M121H]天青蛋白具有三角型1菱形铜位点。