Brown D, Waneck G L
J Am Soc Nephrol. 1992 Oct;3(4):895-906. doi: 10.1681/ASN.V34895.
Many proteins of eukaryotic cells are anchored to membranes by covalent linkage to glycosyl-phosphatidylinositol (GPI). These proteins lack a transmembrane domain, have no cytoplasmic tail, and are, therefore, located exclusively on the extracellular side of the plasma membrane. GPI-anchored proteins form a diverse family of molecules that includes membrane-associated enzymes, adhesion molecules, activation antigens, differentiation markers, protozoan coat components, and other miscellaneous glycoproteins. In the kidney, several GPI-anchored proteins have been identified, including uromodulin (Tamm-Horsfall glycoprotein), carbonic anhydrase type IV, alkaline phosphatase, Thy-1, BP-3, aminopeptidase P, and dipeptidylpeptidase. GPI-anchored proteins can be released from membranes with specific phospholipases and can be recovered from the detergent-insoluble pellet after Triton X-114 treatment of membranes. All GPI-anchored proteins are initially synthesized with a transmembrane anchor, but after translocation across the membrane of the endoplasmic reticulum, the ecto-domain of the protein is cleaved and covalently linked to a preformed GPI anchor by a specific transamidase enzyme. Although it remains obscure why so many proteins are endowed with a GPI anchor, the presence of a GPI anchor does confer some functional characteristics to proteins: (1) it is a strong apical targeting signal in polarized epithelial cells; (2) GPI-anchored proteins do not cluster into clathrin-coated pits but instead are concentrated into specialized lipid domains in the membrane, including so-called smooth pinocytotic vesicles, or caveoli; (3) GPI-anchored proteins can act as activation antigens in the immune system; (4) when the GPI anchor is cleaved by PI-phospholipase C or PI-phospholipase D, second messengers for signal transduction may be generated; (5) the GPI anchor can modulate antigen presentation by major histocompatibility complex molecules. Finally, at least one human disease, paroxysmal nocturnal hemoglobinuria, is a result of defective GPI anchor addition to plasma membrane proteins.
真核细胞的许多蛋白质通过与糖基磷脂酰肌醇(GPI)共价连接而锚定在膜上。这些蛋白质缺乏跨膜结构域,没有胞质尾巴,因此仅位于质膜的细胞外侧。GPI锚定蛋白形成了一个多样化的分子家族,包括膜相关酶、黏附分子、活化抗原、分化标志物、原生动物被膜成分以及其他杂类糖蛋白。在肾脏中,已鉴定出几种GPI锚定蛋白,包括尿调节蛋白(Tamm-Horsfall糖蛋白)、IV型碳酸酐酶、碱性磷酸酶、Thy-1、BP-3、氨肽酶P和二肽基肽酶。GPI锚定蛋白可以用特定的磷脂酶从膜上释放出来,并且在对膜进行Triton X-114处理后可以从去污剂不溶性沉淀中回收。所有GPI锚定蛋白最初都是通过跨膜锚定合成的,但在内质网跨膜转运后,蛋白质的胞外结构域被切割,并通过一种特定的转酰胺酶与预先形成的GPI锚定共价连接。尽管目前尚不清楚为什么这么多蛋白质被赋予GPI锚定,但GPI锚定的存在确实赋予了蛋白质一些功能特性:(1)它是极化上皮细胞中一个强大的顶端靶向信号;(2)GPI锚定蛋白不会聚集到网格蛋白包被小窝中,而是集中在膜中的特殊脂质结构域中,包括所谓的平滑胞饮小泡或小窝;(3)GPI锚定蛋白可以在免疫系统中作为活化抗原;(4)当GPI锚定被PI-磷脂酶C或PI-磷脂酶D切割时,可能会产生信号转导的第二信使;(5)GPI锚定可以调节主要组织相容性复合体分子的抗原呈递。最后,至少有一种人类疾病——阵发性夜间血红蛋白尿,是由于质膜蛋白的GPI锚定添加缺陷所致。