糖基磷脂酰肌醇的合成
中文名称
通路描述
糖基磷脂酰肌醇 (GPI) 作为许多细胞表面蛋白的膜锚定。GPI 在内质网中合成。在人类中,一种包含九个反应的单一路径似乎负责合成参与膜蛋白锚定的主要 GPI 物种。该通路如图示。另外两个未示出的反应允许合成变体形式的 GPI,一种带有额外的甘露糖残基,另一种带有额外的乙醇胺 (Tauon 等人,2004; Shishioh 等人,2005)。这些变体 GPI 分子可用于组织特异性蛋白修饰,或可独立发挥作用。GPI 合成的步骤首先通过分离大量失去表达 GPI 锚定蛋白能力的突变细胞系而确定。对这些细胞系的体细胞杂交分析允许定义对应于不同突变基因的互补组,并基于其在突变细胞中恢复正常细胞表面蛋白表达的能力,鉴定了这些基因的正常形式 cDNA。带有标记的克隆蛋白的共沉淀实验允许鉴定参与 GPI 锚定生物合成的其他蛋白质。
英文描述
Synthesis of glycosylphosphatidylinositol (GPI) Glycosylphosphatidyl inositol (GPI) acts as a membrane anchor for many cell surface proteins. GPI is synthesized in the endoplasmic reticulum. In humans, a single pathway consisting of nine reactions appears to be responsible for the synthesis of the major GPI species involved in membrane protein anchoring. This pathway is shown in the figure. Two additional reactions, not shown, allow the synthesis of variant forms of GPI, one with an additional mannose residue and one with an additional ethanolamine (Tauron et al. 2004; Shishioh et al. 2005). These variant GPI molecules may be used for tissue-specific protein modifications, or may function independently.The steps of GPI synthesis were first identified by isolating large numbers of mutant cell lines that had lost the ability to express GPI anchored proteins on their surfaces. Somatic cell hybrid analyses of these lines allowed the definition of complementation groups corresponding to distinct mutated genes, and cDNAs corresponding to normal forms of these genes were identified on the basis of their abilities to restore normal cell surface protein expression in mutant cells. Co-precipitation experiments with tagged cloned proteins have allowed the identification of additional proteins involved in GPI anchor biosynthesis.
所含基因
18 个基因