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细胞色素c氧化酶的氧化还原滴定:多电子系统分析

Redox titrations of cytochrome c oxidase. An analysis of a multi-electron system.

作者信息

Lanne B, Vänngård T

出版信息

Biochim Biophys Acta. 1978 Mar 13;501(3):449-57. doi: 10.1016/0005-2728(78)90112-3.

Abstract

Equilibrium redox titrations of cytochrome c oxidase available in the literature are discussed in terms of models with interactions both with respect to oxidation-reduction potentials and the particular property studied. 2. The interaction is restricted to be pairwise. For the present data more complicated forms of interaction are not required. In addition, with this limitation a simple matrix formulation can be used. 3. The EPR titrations require potential interaction involving the hemes and the undetectable Cu. In this way the low intensity of the g6 signal can be accounted for. However, it is shown that there is no unique solution to the problem. 4. The optical titrations at 605 nm can be fitted reasonalby well with the potentials from the EPR data with no spectral interaction. 5. Simulated titrations of magnetic susceptibility show a sensitivity to the model chosen indicating the usefulness of future experiments in this area.

摘要

根据有关氧化还原电位和所研究特定性质的相互作用模型,对文献中可得的细胞色素c氧化酶的平衡氧化还原滴定进行了讨论。2. 相互作用被限制为成对的。对于目前的数据,不需要更复杂的相互作用形式。此外,在这种限制下,可以使用简单的矩阵公式。3. EPR滴定需要涉及血红素和不可检测的铜的电位相互作用。通过这种方式,可以解释g6信号的低强度。然而,结果表明该问题没有唯一解。4. 605 nm处的光学滴定可以很好地与来自EPR数据的电位拟合,且没有光谱相互作用。5. 磁化率的模拟滴定显示对所选模型敏感,表明该领域未来实验的有用性。

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