Omura T, Sadano H, Hasegawa T, Yoshida Y, Kominami S
J Biochem. 1984 Nov;96(5):1491-500. doi: 10.1093/oxfordjournals.jbchem.a134978.
Hemoprotein H-450 was purified from rat liver cytosol to homogeneity by an improved procedure. The purified H-450 showed a subunit molecular weight of 64,000 daltons and contained 0.7-0.9 mol of protoheme per mol subunit. Among rat tissues examined, liver and kidney contained significant amounts of H-450 in the cytosol. Oxidized H-450 showed a Soret peak at 428 nm and a broad beta band at around 550 nm. Reduced H-450 was found to exist in two interconvertible forms, alkaline and acid forms. The alkaline form showed Soret, beta, and alpha peaks at 448, 540, and 571 nm, whereas the acid form showed Soret, beta, and alpha peaks at 425, 530, and 558 nm. The spectral properties of both oxidized and reduced H-450 in alkaline medium resemble those of cytochrome P-450 having a nitrogenous ligand at the 6th coordination position of the heme. Upon addition of low concentrations of HgCl2, H-450 was converted to a denatured form both in the oxidized and the reduced states and lost its unique spectral characteristics. Addition of carbon monoxide to reduced H-450 produced a new spectral species which resembled that of the reduced carbon monoxide complex of P-420, a denatured form of cytochrome P-450. Comparison of the EPR signal of oxidized H-450 with those of a cytochrome P-450, P-450(PB-1), and several model compounds indicated the presence of a thiolate anion at the 5th coordination position of the heme of H-450. Judging from EPR data, oxidized H-450 also converts between acid and alkaline forms, whose signals were observed at g = 1.867, 2.31, and 2.507 and at g = 1.910, 2.28, and 2.424, respectively. These lines of evidence indicate that the 5th and 6th coordination positions of the heme of H-450 are a thiolate and a nitrogenous group, respectively. With respect to the heme environments, H-450 is a member of the cytochrome P-450 family, and has a nitrogenous ligand at the 6th coordination position of the heme.
通过改进的方法从大鼠肝脏胞质溶胶中纯化血红蛋白H - 450至均一性。纯化后的H - 450显示亚基分子量为64,000道尔顿,每摩尔亚基含有0.7 - 0.9摩尔原血红素。在所检测的大鼠组织中,肝脏和肾脏的胞质溶胶中含有大量的H - 450。氧化型H - 450在428 nm处有一个Soret峰,在550 nm左右有一个宽的β带。还原型H - 450被发现以两种可相互转化的形式存在,即碱性形式和酸性形式。碱性形式在448、540和571 nm处显示Soret、β和α峰,而酸性形式在425、530和558 nm处显示Soret、β和α峰。氧化型和还原型H - 450在碱性介质中的光谱特性类似于在血红素第6配位位置具有含氮配体的细胞色素P - 450的光谱特性。加入低浓度的HgCl2后,H - 450在氧化态和还原态均转化为变性形式并失去其独特的光谱特征。向还原型H - 450中加入一氧化碳产生了一种新的光谱物种,其类似于P - 420(细胞色素P - 450的一种变性形式)的还原型一氧化碳复合物的光谱。将氧化型H - 450的电子顺磁共振(EPR)信号与细胞色素P - 450、P - 450(PB - 1)以及几种模型化合物的EPR信号进行比较,表明在H - 450血红素的第5配位位置存在硫醇盐阴离子。从EPR数据判断,氧化型H - 450也在酸性和碱性形式之间转化,其信号分别在g = 1.867、2.31和2.507以及g = 1.910、2.28和2.424处观察到。这些证据表明,H - 450血红素的第5和第6配位位置分别是硫醇盐和含氮基团。就血红素环境而言,H - 450是细胞色素P - 450家族的一员,并且在血红素的第6配位位置具有含氮配体。