Doering T L, Masterson W J, Englund P T, Hart G W
Department of Biological Chemistry, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205.
J Biol Chem. 1989 Jul 5;264(19):11168-73.
Non-acetylated glucosamine is an unusual structural feature shared by all glycosyl phosphatidylinositol (GPI) lipids, including a variety of membrane anchors, the leishmanial lipophosphoglycan, and a mediator of insulin action. We proposed previously a pathway for biosynthesis of glycolipid A, the precursor of the GPI membrane anchor of the trypanosome variant surface glycoprotein (Masterson, W. J., Doering, T. L., Hart, G. W., and Englund, P. T. (1989) Cell 56, 793-800). In this paper we characterize in more detail the initial steps of GPI assembly. The first and committed step in the pathway is the transfer of GlcNAc, from UDP-GlcNAc, to endogenous phosphatidylinositol to form N-acetylglucosaminyl phosphatidylinositol (GlcNAc-PI). The GlcNAc-PI is then efficiently deacetylated to form glucosaminyl phosphatidylinositol (GlcN-PI), the substrate for subsequent reactions en route to glycolipid A.
非乙酰化葡糖胺是所有糖基磷脂酰肌醇(GPI)脂质共有的一种特殊结构特征,这些脂质包括多种膜锚定物、利什曼原虫脂磷壁酸以及胰岛素作用的一种介质。我们之前提出了一条糖脂A生物合成途径,糖脂A是锥虫可变表面糖蛋白的GPI膜锚定物的前体(Masterson, W. J., Doering, T. L., Hart, G. W., and Englund, P. T. (1989) Cell 56, 793 - 800)。在本文中,我们更详细地描述了GPI组装的初始步骤。该途径的第一步也是关键步骤是将来自UDP - 葡糖胺的GlcNAc转移到内源性磷脂酰肌醇上,形成N - 乙酰葡糖胺基磷脂酰肌醇(GlcNAc - PI)。然后GlcNAc - PI被有效地脱乙酰化,形成葡糖胺基磷脂酰肌醇(GlcN - PI),它是通往糖脂A后续反应的底物。