Deters D, Hartmann H J, Weser U
Inorganic Biochemistry Department, Eberhard Karls University of Tübingen, Germany.
Biochim Biophys Acta. 1994 Oct 19;1208(2):344-7. doi: 10.1016/0167-4838(94)90123-6.
In an EPR study employing yeast copper(I) thionein, GSH and Cu-GSH it was shown that thiyl radicals could be successfully generated from the thiolate sulfur via oxidation by photochemically formed superoxide at 77 K. The g-value was 2.036. Essentially no EPR detectable copper(II) was monitored under the experimental conditions, indicating that the oxidation reduction process is restricted to the thiolate sulfur. The Cu(I)-thiolate chromophores remained fully intact as deduced from chiroptical and luminescence measurements. Thus, copper thionein is supposed to be actively involved in the scavenging of oxygen free radicals by a reversible thiolate oxidation reduction cycle. The coordinated Cu(I) seems to serve as a prominent candidate to stabilize the transiently formed thiyl radical.
在一项使用酵母铜(I)硫蛋白、谷胱甘肽(GSH)和铜-谷胱甘肽的电子顺磁共振(EPR)研究中,结果表明,在77K下,通过光化学形成的超氧化物氧化,硫醇盐硫可以成功生成硫自由基。g值为2.036。在实验条件下,基本上没有检测到可通过EPR检测的铜(II),这表明氧化还原过程仅限于硫醇盐硫。从圆二色光谱和发光测量结果推断,铜(I)-硫醇盐发色团保持完全完整。因此,推测铜硫蛋白通过可逆的硫醇盐氧化还原循环积极参与清除氧自由基。配位的铜(I)似乎是稳定瞬时形成的硫自由基的主要候选者。