Department of Biochemistry and Molecular Biology, Indiana University School of Medicine, Indianapolis, IN 46202, USA.
Cell Metab. 2011 Mar 2;13(3):274-82. doi: 10.1016/j.cmet.2011.01.017.
Glycogen is a branched polymer of glucose that serves as an energy store. Phosphate, a trace constituent of glycogen, has profound effects on glycogen structure, and phosphate hyperaccumulation is linked to Lafora disease, a fatal progressive myoclonus epilepsy that can be caused by mutations of laforin, a glycogen phosphatase. However, little is known about the metabolism of glycogen phosphate. We demonstrate here that the biosynthetic enzyme glycogen synthase, which normally adds glucose residues to glycogen, is capable of incorporating the β-phosphate of its substrate UDP-glucose at a rate of one phosphate per approximately 10,000 glucoses, in what may be considered a catalytic error. We show that the phosphate in glycogen is present as C2 and C3 phosphomonoesters. Since hyperphosphorylation of glycogen causes Lafora disease, phosphate removal by laforin may thus be considered a repair or damage control mechanism.
糖原是葡萄糖的支链聚合物,可作为能量储存。磷酸是糖原的痕量成分,对糖原结构有深远影响,而磷酸的过度积累与拉福拉病有关,拉福拉病是一种致命的进行性肌阵挛癫痫,可由糖原磷酸酶的 laforin 突变引起。然而,关于糖原磷酸的代谢知之甚少。我们在这里证明,通常将葡萄糖残基添加到糖原中的生物合成酶糖原合酶能够以大约每 10000 个葡萄糖一个磷酸的速率掺入其底物 UDP-葡萄糖的β-磷酸,这可能被视为一种催化错误。我们表明,糖原中的磷酸以 C2 和 C3 磷酸单酯的形式存在。由于糖原的过度磷酸化会导致拉福拉病,因此 laforin 通过去除磷酸可以被认为是一种修复或损伤控制机制。