汞(II)-谷胱甘肽偶联物的形成使用高质量精度质谱检测。

Zachary Fine, Troy D Wood
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引用次数: 4

摘要

孕妇在怀孕期间暴露于汞(II)已被确定为严重神经行为障碍发展的潜在因果因素。自闭症儿童的还原性谷胱甘肽(GSH)/氧化谷胱甘肽(GSSG)比例较低,并且已知GSH与汞(II)有很强的结合。为了深入了解GSH结合Hg(II)的机制,采用高分辨率质谱联用串联质谱法研究了GSH与Hg(II)的结合过程。虽然在Hg(II)和GSH的水溶液混合后不会立即形成1:1的Hg(II):GSH共轭物,但可以观察到两种含有Hg(II)的物质:1:2 Hg(II):GSH共轭物[(GS)2Hg + H+]和第二种含有Hg(II)的物质,约m/z 544。有趣的是,该物种在m/z 544处随时间减少,而1:1 Hg(II):GSH共轭物的存在增加,这表明m/z 544是1:1共轭物形成的中间物。利用傅里叶变换离子回旋共振(FT-ICR)质谱与电喷雾电离源耦合的高质量精度的实验表明,中间物质是[GSH + HgCl]+,而不是先前文献中假设的1:1共轭物[Hg(GSH) - H + 2H2O]+。碰撞诱导解离实验进一步证实了[GSH + HgCl]+的存在,表明中间HCl的中性损失以及N端和c端氨基酸的损失,表明Hg(II)在Cys残基上结合。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Formation of Mercury(II)-Glutathione Conjugates Examined Using High Mass Accuracy Mass Spectrometry.

Maternal exposure to Hg(II) during pregnancy has been identified as a potential causal factor in the development of severe neurobehavioral disorders. Children with autism have been identified with lower reduced glutathione (GSH)/oxidized glutathione (GSSG) ratios, and GSH is known to strongly bind Hg(II). In order to gain insight into the mechanism by which GSH binds Hg(II), high resolution mass spectrometry coupled with tandem mass spectrometry was utilized to examine the conjugation process. While the 1:1 Hg(II):GSH conjugate is not formed immediately upon mixing aqueous solutions of Hg(II) and GSH, two species containing Hg(II) are observed: the 1:2 Hg(II):GSH conjugate, [(GS)2Hg + H+], and a second Hg(II)-containing species around m/z 544. Interestingly, this species at m/z 544 decreases in time while the presence of the 1:1 Hg(II):GSH conjugate increases, suggesting that m/z 544 is an intermediate in the formation of the 1:1 conjugate. Experiments using the high mass accuracy capability of Fourier transform ion cyclotron resonance (FT-ICR) mass spectrometry coupled to an electrospray ionization source indicate that the intermediate species is [GSH + HgCl]+, and not the 1:1 conjugate [Hg(GSH) - H + 2H2O]+ postulated in previous literature. Further confirmation of [GSH + HgCl]+ is supported by collision of induced dissociation experiments, which show neutral loss of HCl from the intermediate and loss of the N- and C-terminal amino acids, indicating binding of Hg(II) at the Cys residue.

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