Wilson M T, Antonini G, Malatesta F, Sarti P, Brunori M
Department of Chemistry and Biological Chemistry, University of Essex, Colchester, United Kingdom.
J Biol Chem. 1994 Sep 30;269(39):24114-9.
Cyanide binding to cytochrome c oxidase has been investigated by sequential mixing and rapid scan stopped flow spectroscopy. Double mixing experiments confirm earlier reports that cyanide binds rapidly to partially reduced enzyme species formed in turnover. The absorbance/time/wavelength matrices, captured during the onset of cyanide inhibition of cytochrome c oxidase by rapid scan stopped flow, were analyzed by singular value decomposition and the spectral contributions of the chromophores separated. Examination of the time courses and amplitudes of the spectral signals provide evidence that entry of a single (1-1.3) electron into the enzyme is sufficient to trigger rapid cyanide binding. This electron resides predominantly on the cytochrome a/CuA pair in the inhibited enzyme. In addition, although cytochrome a3 remains oxidized, it does not appear to be the site for the initial inhibitory binding of cyanide. Our data suggest that CuB2+ is the initial binding site.
已通过顺序混合和快速扫描停流光谱法研究了氰化物与细胞色素c氧化酶的结合。双混合实验证实了早期的报道,即氰化物与周转过程中形成的部分还原的酶物种迅速结合。通过奇异值分解分析了在快速扫描停流法对细胞色素c氧化酶进行氰化物抑制开始时捕获的吸光度/时间/波长矩阵,并分离了发色团的光谱贡献。对光谱信号的时间进程和幅度的检查提供了证据,即单个(1-1.3)电子进入酶足以触发氰化物的快速结合。该电子主要存在于受抑制酶中的细胞色素a/CuA对中。此外,尽管细胞色素a3保持氧化状态,但它似乎不是氰化物初始抑制结合的位点。我们的数据表明CuB2+是初始结合位点。