Biosynthesis of glycosylphosphatidylinositols in mammals and unicellular microbes

被引:85
作者
Tiede, A
Bastisch, I
Schubert, J
Orlean, P
Schmidt, RE [1 ]
机构
[1] Hannover Med Sch, Dept Clin Immunol, D-30625 Hannover, Germany
[2] Univ Illinois, Dept Biochem, Urbana, IL 61801 USA
关键词
drug design; glycoprotein; glycosylphosphatidylinositol; GPI anchor; paroxysmal nocturnal hemoglobinuria; posttranslational modification;
D O I
10.1515/BC.1999.066
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Membrane anchoring of cell surface proteins via glycosylphosphatidylinositol (GPI) occurs in all eukaryotic organisms. In addition, GPI-related glycophospholipids are important constituents of the glycan coat of certain protozoa, Defects in GPI biosynthesis can retard, if not abolish growth of these organisms. In humans, a defect in GPI biosynthesis can cause paroxysmal nocturnal hemoglobinuria (PNH), a severe acquired bone marrow disorder. Here, we review advances in the characterization of GPI biosynthesis in parasitic protozoa, yeast and mammalian cells. The GPI core structure as well as the major steps in its biosynthesis are conserved throughout evolution. However, there are significant biosynthetic differences between mammals and microbes. First indications are that these differences could be exploited as targets in the design of novel pharmacotherapeutics that selectively inhibit GPI biosynthesis in unicellular microbes.
引用
收藏
页码:503 / 523
页数:21
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