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Plasmodium falciparum and P. knowlesi: initial identification and characterization of malaria synthesized glycolipids
Authors:J A Sherwood  S L Spitalnik  S B Aley  I A Quakyi  R J Howard
Institution:1. Department of Immunopathology, Sanquin Research, Landsteiner Laboratory of the Academic Medical Center, University of Amsterdam, Plesmanlaan 125, 1066 CX Amsterdam, The Netherlands;2. Department of Hematology, Academic Medical Center, University of Amsterdam, Meibegdreef 9, 1105 AZ Amsterdam, The Netherlands;1. Technology Transfer and Innovation Support Office, Institutional Office, North-West Univerity, Private Bag X1290, 2520 Potchefstroom, South Africa;2. Department of Health Science, Faculty of Health and Environmental, Biomedical Technology, Central University of Technology, Free State, Private Bag X20539, 9300 Bloemfontein, South Africa;3. Indigenous Knowledge Systems Centre, Faculty of Natural and Agricultural Sciences, North-West University, Mmabatho 2790, South Africa
Abstract:This is the first report establishing the existence of glycolipids synthesized by plasmodia, in particular Plasmodium falciparum. Trophozoites, schizonts, gametocytes, and gametes were metabolically labeled in vitro with 3H]glucosamine, 3H]galactose, 3H]glucose, 3H]mannose, 3H]fucose, 32P]inorganic phosphate, or 35S]sulfate, and total lipid extracts analyzed by high-performance thin-layer chromatography and autoradiography or fluorography. Parasites incorporated 3H]monosaccharides into distinctly different series of molecules previously undescribed. Three properties of 3H]glucosamine labeled molecules indicate they are glycolipids. First, labeled molecules have lipid solubility properties. Second, mobility on thin-layer chromatography was characteristic of glycolipids. Third, following acid hydrolysis, 3H]glucosamine was recovered from a total lipid extract of labeled parasites demonstrating that glucosamine is a constituent of some of these lipid molecules. Most of these glycolipids are neutral and alkali labile. The majority of these glycolipids differs from several synthesized phospholipids. None of these glycolipids was sulfated. Plasmodial glycolipid synthesis occurs concomitantly with glycoprotein synthesis, and both increase during schizogony. Many of these glycolipids appear to be identical among three strains of P. falciparum and between two species, P. falciparum and P. knowlesi. In contrast, there are stage specific differences in glycolipid synthesis among rings, schizonts, gametocytes, and a mixture of gametes plus zygotes of P. falciparum, examples of both erythrocytic and vector forms of the parasite.
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