Zhang B, Tang W, Gao S, Zhou Y
State Key Laboratory of Coordination Chemistry, Nanjing University, People's Republic of China.
J Inorg Biochem. 1995 Apr;58(1):9-19. doi: 10.1016/0162-0134(94)00031-5.
The first observation of the circular dichroism (CD) spectral features of platinum-saturated metallothionein, Pt7MT, is presented. It is characterized by two intensive bands with maxima at 235 nm (-) and 255 nm (+). Properties of the reactions of cis- and trans-diamminedichloroplatinum (DDP) with rabbit liver MT have been studied by monitoring the CD spectral changes. The overall rate of the reaction between trans-DDP and MT is determined to be significantly faster than that for cis-DDP and MT. The stepwise incorporation of Pt into Zn7MT resulted in a nonsystemic changes in the CD spectral envelope. These data argue that Pt(II) replaces Zn(II) in ZnMT in a nonspecific, "distributed" manner across both domains, because the onset of clustering was observed after 5 mol equiv of Pt was bound. A dynamic mechanism has been proposed in which the reaction proceeds via the formation of an intermediate, RS-Pt (NH3)2-SR. As it is converted to the product, the ammine ligands are lost very slowly, especially in the case of cis-DDP, because of the strong requirement of Pt for square planar coordination, which comprises the rate-limiting step.
首次报道了铂饱和金属硫蛋白Pt7MT的圆二色性(CD)光谱特征。其特征在于在235nm(-)和255nm(+)处有两个强吸收带。通过监测CD光谱变化研究了顺式和反式二氯二氨合铂(DDP)与兔肝MT的反应特性。确定反式DDP与MT之间反应的总速率明显快于顺式DDP与MT之间的反应速率。将Pt逐步掺入Zn7MT中导致CD光谱包络发生非系统性变化。这些数据表明,Pt(II)以非特异性的“分布”方式取代了ZnMT中两个结构域的Zn(II),因为在结合5摩尔当量的Pt后观察到了聚集现象。提出了一种动力学机制,其中反应通过中间体RS-Pt(NH3)2-SR的形成进行。当它转化为产物时,氨配体的丢失非常缓慢,特别是在顺式DDP的情况下,因为Pt对方形平面配位有强烈要求,这构成了限速步骤。