Jensen P, Wilson M T, Aasa R, Malmström B G
Biochem J. 1984 Dec 15;224(3):829-37. doi: 10.1042/bj2240829.
The inhibition of cytochrome c oxidase by cyanide, starting either with the resting or the pulsed enzyme, was studied by rapid-freeze quenching followed by quantitative e.p.r. It is found that a partial reduction of cytochrome oxidase by transfer of 2 electron equivalents from ferrocytochrome c to cytochrome a and CuA will induce a transition from a closed to an open enzyme conformation, rendering the cytochrome a3-CuB site accessible for cyanide binding, possibly as a bridging ligand. A heterogeneity in the enzyme is observed in that an e.p.r. signal from the cytochrome a3 3+-HCN complex is only found in 20% of the molecules, whereas the remaining cyanide-bound a3-CuB sites are e.p.r.-silent.
通过快速冷冻淬灭随后进行定量电子顺磁共振研究了氰化物对细胞色素c氧化酶的抑制作用,起始酶状态为静止或脉冲状态。研究发现,通过将2个电子当量从亚铁细胞色素c转移到细胞色素a和铜A,细胞色素氧化酶的部分还原会诱导从封闭到开放的酶构象转变,使细胞色素a3-CuB位点可用于氰化物结合,氰化物可能作为桥连配体。观察到该酶存在异质性,即仅在20%的分子中发现细胞色素a3 3+-HCN复合物的电子顺磁共振信号,而其余与氰化物结合的a3-CuB位点在电子顺磁共振中无信号。