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
相关论文
共 170 条
[1]   TOPOGRAPHY OF GLYCOSYLATION REACTIONS IN THE ENDOPLASMIC-RETICULUM [J].
ABEIJON, C ;
HIRSCHBERG, CB .
TRENDS IN BIOCHEMICAL SCIENCES, 1992, 17 (01) :32-36
[2]  
[Anonymous], WORLD HLTH REP
[3]   CAMP-MEDIATED PROTEIN-PHOSPHORYLATION OF MICROSOMAL-MEMBRANES INCREASES MANNOSYLPHOSPHODOLICHOL SYNTHASE ACTIVITY [J].
BANERJEE, DK ;
KOUSVELARI, EE ;
BAUM, BJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (18) :6389-6393
[4]   THE SACCHAROMYCES-CEREVISIAE DPM1 GENE ENCODING DOLICHOL-PHOSPHATE-MANNOSE SYNTHASE IS ABLE TO COMPLEMENT A GLYCOSYLATION-DEFECTIVE MAMMALIAN-CELL LINE [J].
BECK, PJ ;
ORLEAN, P ;
ALBRIGHT, C ;
ROBBINS, PW ;
GETHING, MJ ;
SAMBROOK, JF .
MOLECULAR AND CELLULAR BIOLOGY, 1990, 10 (09) :4612-4622
[5]   COMPLEMENTING MUTANT ALLELES DEFINE 3 LOCI INVOLVED IN MANNOSYLATION OF MAN(5)-GLCNAC(2)-P-P-DOLICHOL IN CHINESE-HAMSTER OVARY CELLS [J].
BECK, PJ ;
GETHING, MJ ;
SAMBROOK, J ;
LEHRMAN, MA .
SOMATIC CELL AND MOLECULAR GENETICS, 1990, 16 (06) :539-548
[6]   IDENTIFICATION OF 6 COMPLEMENTATION CLASSES INVOLVED IN THE BIOSYNTHESIS OF GLYCOSYLPHOSPHATIDYLINOSITOL ANCHORS IN SACCHAROMYCES-CEREVISIAE [J].
BENGHEZAL, M ;
LIPKE, PN ;
CONZELMANN, A .
JOURNAL OF CELL BIOLOGY, 1995, 130 (06) :1333-1344
[7]   Yeast gpi8p is essential for GPI anchor attachment onto proteins [J].
Benghezal, M ;
Benachour, A ;
Rusconi, S ;
Aebi, M ;
Conzelmann, A .
EMBO JOURNAL, 1996, 15 (23) :6575-6583
[8]   GENOMIC ORGANIZATION OF THE X-LINKED GENE (PIG-A) THAT IS MUTATED IN PAROXYSMAL-NOCTURNAL HEMOGLOBINURIA AND OF A RELATED AUTOSOMAL PSEUDOGENE MAPPED TO 12Q21 [J].
BESSLER, M ;
HILLMEN, P ;
LONGO, L ;
LUZZATTO, L ;
MASON, PJ .
HUMAN MOLECULAR GENETICS, 1994, 3 (05) :751-757
[9]   PAROXYSMAL-NOCTURNAL HEMOGLOBINURIA (PNH) IS CAUSED BY SOMATIC MUTATIONS IN THE PIG-A GENE [J].
BESSLER, M ;
MASON, PJ ;
HILLMEN, P ;
MIYATA, T ;
YAMADA, N ;
TAKEDA, J ;
LUZZATTO, L ;
KINOSHITA, T .
EMBO JOURNAL, 1994, 13 (01) :110-117
[10]   Lipophosphoglycan (LPG) and the identification of virulence genes in the protozoan parasite Leishmania [J].
Beverley, SM ;
Turco, SJ .
TRENDS IN MICROBIOLOGY, 1998, 6 (01) :35-40