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进一步探讨天青蛋白的电荷转移跃迁和星鸦胆素配体部分。

Further perspectives on the charge transfer transitions of blue copper proteins and the ligand moieties in stellacyanin.

机构信息

Department of Chemistry, Purdue University, West Lafayette, Indiana 47907.

出版信息

Proc Natl Acad Sci U S A. 1981 Nov;78(11):6567-70. doi: 10.1073/pnas.78.11.6567.

Abstract

The charge transfer spectra of plastocyanin and azurin are analyzed in detail, taking into account the structural information that is available. The number and relative energies of the low-lying charge transfer bands attributable to cysteine and methionine sulfur are considered with reference to the energy levels associated with the donor centers and to experimental work on relevant complexes. Two cysteine --> Cu(II) charge transfer transitions are assigned to bands that occur near 620 nm and near 770 nm. Energy considerations suggest that the methionine --> Cu(II) transition occurs in the vicinity of 550 nm for both plastocyanin and azurin. The existence of a disulfide linkage in stellacyanin is established by thiol titrations, and the possibility exists that the fourth ligand in stellacyanin may involve disulfide sulfur. If so, the cystine --> Cu(II) transition is also expected to appear around 550 nm.

摘要

详细分析了质体蓝素和蓝铜蛋白的电荷转移光谱,同时考虑了可用的结构信息。参考与供体中心相关的能级以及相关配合物的实验工作,考虑了归因于半胱氨酸和蛋氨酸硫的低电荷转移带的数量和相对能量。将两个半胱氨酸-> Cu(II)电荷转移跃迁分配给在 620nm 附近和 770nm 附近发生的带。能量考虑表明,对于质体蓝素和蓝铜蛋白,蛋氨酸-> Cu(II)跃迁发生在 550nm 附近。通过巯基滴定法确定星形蛋白中存在二硫键连接,并且星形蛋白中的第四个配体可能涉及二硫键硫。如果是这样,半胱氨酸-> Cu(II)跃迁也预计出现在 550nm 左右。

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