Herve M, Garnier A, Tosi L, Steinbuch M
Biochim Biophys Acta. 1976 Aug 9;439(2):432-41. doi: 10.1016/0005-2795(76)90080-5.
The effect of anion binding to ceruloplasmin has been studied using absorption and cirbular dichroism spectral data. At anion to ceruloplasmin molar ratios approaching infinite, OCN-, N3- and SCN- bind to ceruloplasmin giving rise to similar alterations in circular dichroism and absorption spectra. The positive bands at 610 and 520 nm in circular dichroism spectra disappear, a negative one apperars at 600 nm and the peak at 450 nm is only slightly modified. There is a new negative band at 410 nm well-defined in OCN- ceruloplasmin spectra. The decrease in absorption at 610 nm is ascribed to the disruption of one type I Cu-S(cysteine) bond owing presumably to the changes induced by anions in the protein secondary structure. The new band at 410 nm is assigned to a charge transfer transition from the ligand replacing cysteine at its binding site. Both absorption and circular dichroism spectra show isobestic points indicating that anion binding to the enzyme, disruption of one of the two type I Cu-S bonds and coordination of this Cu to another protein residue take place simultaneously.
利用吸收光谱和圆二色光谱数据研究了阴离子与铜蓝蛋白结合的效应。在阴离子与铜蓝蛋白的摩尔比接近无穷大时,氰酸根离子(OCN⁻)、叠氮根离子(N₃⁻)和硫氰酸根离子(SCN⁻)与铜蓝蛋白结合,在圆二色光谱和吸收光谱中产生相似的变化。圆二色光谱中610和520 nm处的正峰消失,600 nm处出现一个负峰,450 nm处的峰仅略有改变。在氰酸根离子 - 铜蓝蛋白光谱中,410 nm处出现一个新的清晰的负峰。610 nm处吸收的降低归因于一种I型铜 - 硫(半胱氨酸)键的破坏,这可能是由于阴离子引起的蛋白质二级结构变化所致。410 nm处的新峰归因于从取代其结合位点半胱氨酸的配体发生的电荷转移跃迁。吸收光谱和圆二色光谱均显示等吸收点,表明阴离子与该酶的结合、两个I型铜 - 硫键之一的破坏以及该铜与另一个蛋白质残基的配位同时发生。