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Efficient Oxidation and Destabilization of Zn(Cys)4 Zinc Fingers by Singlet Oxygen

机译:单重态氧对Zn(Cys)4锌指的有效氧化和去稳定作用

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Singlet oxygen (~1O2) plays an important role in oxidative stress in all types of organisms, most of them being able to mount a defense against this oxidant. Recently, zinc finger proteins have been proposed to be involved in its cellular detection but the molecular basis of this process still remains unknown. We have studied the reactivity of a Zn(Cys)4 zinc finger with ~1O2 by combinations of spectroscopic and analytical techniques, focusing on the products formed and the kinetics of the reaction. We report that the cysteines of this zinc finger are oxidized to sulfonates by ~1O2. The reaction of the ZnS4 core with ~1O2 is very fast and efficient with almost no physical quenching of ~1O2 A drastic (ca. five orders of magnitude) decrease of the Zn~(2+) binding constant was observed upon oxidation. This suggests that the Zn(Cys)4 zinc finger proteins would release their Zn~(2+) ion and unfold upon reaction with ~1O2 under cellular conditions and that zinc finger sites are likely targets for ~1O2.
机译:单线态氧(〜1O2)在所有类型的生物体的氧化应激中都起着重要作用,其中大多数能够防御这种氧化剂。近来,已经提出锌指蛋白参与其细胞检测,但是该过程的分子基础仍然未知。我们已经结合光谱学和分析技术研究了Zn(Cys)4锌指与〜1O2的反应性,重点研究了形成的产物和反应动力学。我们报道该锌指的半胱氨酸被〜1O2氧化为磺酸盐。 ZnS4核与〜1O2的反应非常快速有效,几乎没有〜1O2的物理淬灭。氧化后观察到Zn〜(2+)结合常数急剧下降(大约五个数量级)。这表明Zn(Cys)4锌指蛋白会在细胞条件下与〜1O2反应时释放其Zn〜(2+)离子并展开,并且锌指位点可能是〜1O2的靶标。

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