Glycoinositolphospholipids, free and as anchors of proteins, in Trypanosoma cruzi

被引:34
作者
de Lederkremer, RM [1 ]
Bertello, LE [1 ]
机构
[1] Univ Buenos Aires, Fac Ciencias Exactas & Nat, Dept Quim Organ, CIHIDECAR, RA-1428 Buenos Aires, DF, Argentina
关键词
D O I
10.2174/1381612013397519
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The most important glycoproteins of trypanosomatids are anchored by glycoinositolphospholipids (GIPLs) to their plasma membrane. In addition, free GIPLs have been described, for instance the lipopeptidophosphoglycan (LPPG) which is a major component of the surface of T. cruzi epimastigotes. An inositolphosphoceramide (IPC) is part of the LPPG and of glycoproteins present in different stages of T. cruzi. Ceramide was not found in mammal GIPL-anchors. The lipid moieties in T. cruzi anchors can be quite variable. However, mo diacylglycerol (DAG) was found in contrast with the African trypanosomes. In GIPLs of epimastigotes collected at the logarithmic phase of growth both, 1 -O-hexadecyl-2-O-palmitoylglycerol and ceramide were identified. Lignoceroylsphinganine is the major ceramide, however, no lignoceric acid was detected when analysing the candidate precursors IPCs, in any of the stages of T. cruzi. An alkylglycerol has been found either as a lyse species in the Tc85 glycoprotein of trypomastigotes or acylated as in the 1G7 anchor of metacyclic forms and in the mucins of epimastigote forms. The lipid in the mucins is replaced by ceramide when the parasite differentiates to metacyclic forms. Also, in the Ssp-4 glycoprotein characteristic of amastigotes, a ceramide was identified as the anchor lipid. These variations suggest that a remodelling mechanism is working in T. cruzi. On the other hand, the oligosaccharide core in the GIPLs of T. cruzi is substituted with galactofuranose, This monosaccharide is found only in the pyranose configuration in mammalian glycoproteins and glycolipids. Thus, the biosynthetic steps for the introduction of galactofuranose and ceramide in the anchors of T. cruzi are good targets for the development of therapeutic agents.
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页码:1165 / 1179
页数:15
相关论文
共 101 条
[41]   First synthesis of beta-D-Galf(1-4)GlcNAc, a structural unit attached o-glycosidically in glycoproteins of Trypanosoma cruzi [J].
GalloRodriguez, C ;
Varela, O ;
deLederkremer, RM .
JOURNAL OF ORGANIC CHEMISTRY, 1996, 61 (05) :1886-1889
[42]   Glycosylphosphatidylinositols are required for the development of Trypanosoma cruzi amastigotes [J].
Garg, N ;
Postan, M ;
MensaWilmot, K ;
Tarleton, RL .
INFECTION AND IMMUNITY, 1997, 65 (10) :4055-4060
[43]   Proteins with glycosylphosphatidylinositol (GPI) signal sequences have divergent fates during a GPI deficiency - GPIs are essential for nuclear division in Trypanosoma cruzi [J].
Garg, N ;
Tarleton, RL ;
MensaWilmot, K .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (19) :12482-12491
[44]   Glycosyl-phosphatidylinositols of Trypanosoma congolense: Two common precursors but a new protein-anchor [J].
Gerold, P ;
Striepen, B ;
Reitter, B ;
Geyer, H ;
Geyer, R ;
Reinwald, E ;
Risse, HJ ;
Schwarz, RT .
JOURNAL OF MOLECULAR BIOLOGY, 1996, 261 (02) :181-194
[45]   Cloning of a surface membrane glycoprotein specific for the infective form of Trypanosoma cruzi having adhesive properties to laminin [J].
Giordano, R ;
Fouts, DL ;
Tewari, D ;
Colli, W ;
Manning, JE ;
Alves, MJM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (06) :3461-3468
[46]  
Gomes NA, 1996, J IMMUNOL, V156, P628
[47]   TRYPANOSOMA-CRUZI - SHEDDING OF SURFACE-ANTIGENS AS MEMBRANE-VESICLES [J].
GONCALVES, MF ;
UMEZAWA, ES ;
KATZIN, AM ;
DESOUZA, W ;
ALVES, MJM ;
ZINGALES, B ;
COLLI, W .
EXPERIMENTAL PARASITOLOGY, 1991, 72 (01) :43-53
[48]  
GUTHER MLS, 1994, J BIOL CHEM, V269, P18694
[49]  
GUTHER MLS, 1992, J BIOL CHEM, V267, P6820
[50]  
HANNUN YA, 1994, J BIOL CHEM, V269, P3125