Total synthesis of the fully lipidated glycosylphosphatidylinositol (GPI) anchor of malarial parasite Plasmodium falciparum

被引:19
作者
Ali, Asif [1 ]
Vishwakarma, Ram A. [1 ,2 ]
机构
[1] Natl Inst Immunol, Bioorgan Chem Lab, New Delhi 110067, India
[2] CSIR, Div Med Chem, Indian Inst Integrat Med, Jammu 180001, India
关键词
Glycosylphosphatidylinositol; GPI anchor; Malaria; Plasmodium falciparum; PROTEIN-KINASE-C; TRYPANOSOMA-BRUCEI; LEISHMANIA PARASITE; CHEMICAL-SYNTHESIS; SOLID-PHASE; FLIP-FLOP; PHOSPHATIDYLINOSITOL; MEMBRANE; PHOSPHOGLYCANS; PATHOGENESIS;
D O I
10.1016/j.tet.2010.04.014
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
We report a new and convergent strategy for the total synthesis of fully lipidated glycosylphosphatidylinositol (GPI) anchor, the major pro-inflammatory factor of malarial parasite (Plasmodium falciparum). The key features of our approach include, the access to the key glucosamine-inositol intermediate by a novel route without a priori resolution of myo-inositol, convergent assembly of the tetramannose glycan domain, flexibility for the placement of the three fatty acids in the desired order in the final steps, and the opportunity to construct GPI analogues/mimics to probe the biosynthesis, immunology and cell biology of the GPI anchor pathway in the malaria parasite. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4357 / 4369
页数:13
相关论文
共 35 条
[1]   A new approach to construct full-length glycosylphosphatidylinositols of parasitic protozoa and [4-deoxy-Man-III]-GPI analogues [J].
Ali, A ;
Gowda, DC ;
Vishwakarma, RA .
CHEMICAL COMMUNICATIONS, 2005, (04) :519-521
[2]  
Baeschlin DK, 2000, CHEM-EUR J, V6, P172, DOI 10.1002/(SICI)1521-3765(20000103)6:1<172::AID-CHEM172>3.0.CO
[3]  
2-5
[4]   FIRST SYNTHESIS OF A FULLY PHOSPHORYLATED GPI MEMBRANE ANCHOR - RAT-BRAIN THY-1 [J].
CAMPBELL, AS ;
FRASERREID, B .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1995, 117 (41) :10387-10388
[5]   Alkylacylglycerolipid domain of GPI molecules of Leishmania is responsible for inhibition of PKC-mediated c-fos expression [J].
Chawla, M ;
Vishwakarma, RA .
JOURNAL OF LIPID RESEARCH, 2003, 44 (03) :594-600
[6]   Synthesis of α-Manp-(1→2)-α-Manp-(1→3)-α-Manp-(1→3)-Manp, the tetrasaccharide repeating unit of Escherichia coli O9a, and α-Manp-(1→2)-α-Manp-(1→2)-α-Manp-(1→3)-α-Manp-(1→3)-Manp, the pentasaccharide repeating unit of E-coli O9 and Klebsiella O3 [J].
Chen, LQ ;
Zhu, YL ;
Kong, FZ .
CARBOHYDRATE RESEARCH, 2002, 337 (05) :383-390
[7]   PARASITE GLYCOCONJUGATES .1. THE SYNTHESIS OF SOME EARLY AND RELATED INTERMEDIATES IN THE BIOSYNTHETIC-PATHWAY OF GLYCOSYL-PHOSPHATIDYLINOSITOL MEMBRANE ANCHORS [J].
COTTAZ, S ;
BRIMACOMBE, JS ;
FERGUSON, MAJ .
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1993, (23) :2945-2951
[8]   A facile synthesis of per-O-alkylated glycono-delta-lactones from per-O-alkylated glycopyranosides and a novel ring contraction for pyranoses [J].
Goebel, M ;
Nothofer, HG ;
Ross, G ;
Ugi, I .
TETRAHEDRON, 1997, 53 (09) :3123-3134
[9]   Nanoclusters of GPI-Anchored Proteins Are Formed by Cortical Actin-Driven Activity [J].
Goswami, Debanjan ;
Gowrishankar, Kripa ;
Bilgrami, Sameera ;
Ghosh, Subhasri ;
Raghupathy, Riya ;
Chadda, Rahul ;
Vishwakarma, Ram ;
Rao, Madan ;
Mayor, Satyajit .
CELL, 2008, 135 (06) :1085-1097
[10]   Rapid synthesis of a glycosylphosphatidylinositol-based malaria vaccine using automated solid-phase oligosaccharide synthesis [J].
Hewitt, MC ;
Snyder, DA ;
Seeberger, PH .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2002, 124 (45) :13434-13436