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谷胱甘肽通过形成双环[4.4.1]十一烷加合物来捕获甲醛。

Glutathione traps formaldehyde by formation of a bicyclo[4.4.1]undecane adduct.

作者信息

Bateman Raynard, Rauh Daniel, Shokat Kevan M

机构信息

Howard Hughes Medical Institute, Department of Cellular and Molecular Pharmacology, UCSF, 600 16th St., San Francisco, CA 94143-2280, USA.

出版信息

Org Biomol Chem. 2007 Oct 21;5(20):3363-7. doi: 10.1039/b707602a. Epub 2007 Aug 29.

Abstract

Glutathione forms complex reaction products with formaldehyde, which can be further modified through enzymatic modification. We studied the non-enzymatic reaction between glutathione and formaldehyde and identified a bicyclic complex containing two equivalents of formaldehyde and one glutathione molecule by protein X-ray crystallography (PDB accession number 2PFG). We have also used (1)H, (13)C and 2D NMR spectroscopy to confirm the structure of this unusual adduct. The key feature of this adduct is the involvement of the gamma-glutamyl alpha-amine and the Cys thiol in the formation of the bicyclic ring structure. These findings suggest that the structure of GSH allows for bi-dentate masking of the reactivity of formaldehyde. As this species predominates at near physiological pH values, we suggest this adduct may have biological significance.

摘要

谷胱甘肽与甲醛形成复杂的反应产物,该产物可通过酶促修饰进一步改变。我们研究了谷胱甘肽与甲醛之间的非酶促反应,并通过蛋白质X射线晶体学(蛋白质数据银行登录号2PFG)鉴定出一种含有两当量甲醛和一个谷胱甘肽分子的双环复合物。我们还使用了氢-1、碳-13和二维核磁共振光谱来确认这种不寻常加合物的结构。该加合物的关键特征是γ-谷氨酰α-胺和半胱氨酸硫醇参与双环结构的形成。这些发现表明,谷胱甘肽的结构允许对甲醛的反应性进行双齿掩蔽。由于该物种在接近生理pH值时占主导地位,我们认为这种加合物可能具有生物学意义。

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