Censullo P, Davitz M A
Division of Immunology, New York University School of Medicine, New York 10016.
Braz J Med Biol Res. 1994 Feb;27(2):289-95.
Glycosylphosphatidylinositol (GPI)-anchored proteins comprise a diverse class of membrane molecules. They protect cells from complement-mediated lysis, control cell to cell adhesion, activate T cells, and play a role in the etiology of slow viral diseases. Despite their functional diversity, GPI-anchored proteins are all attached to the plasma membrane by a common glycolipid anchor. We will examine one aspect of GPI-anchor metabolism, namely, the processing of the molecule after it arrives at the plasma membrane. After biosynthesis and transport to the plasma membrane, the GPI-anchored protein can be endocytosed and degraded or cleaved and released. The enzymatic machinery controlling the catabolism of GPI-anchored molecules at the plasma membrane is likely to play a central role in regulating the cell surface expression of these molecules.
糖基磷脂酰肌醇(GPI)锚定蛋白构成了一类多样的膜分子。它们保护细胞免受补体介导的裂解,控制细胞间粘附,激活T细胞,并在慢病毒疾病的病因学中发挥作用。尽管它们功能多样,但GPI锚定蛋白都通过一个共同的糖脂锚定连接到质膜上。我们将研究GPI锚定代谢的一个方面,即该分子到达质膜后的加工过程。在生物合成并转运到质膜后,GPI锚定蛋白可以被内吞并降解或裂解并释放。控制质膜上GPI锚定分子分解代谢的酶机制可能在调节这些分子的细胞表面表达中起核心作用。