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Synthesis of the Trypanosoma cruzi LPPG heptasaccharyl myo-inositol
Linköpings universitet, Institutionen för fysik, kemi och biologi, Kemi. Linköpings universitet, Tekniska högskolan.
Linköpings universitet, Institutionen för fysik, kemi och biologi, Kemi. Linköpings universitet, Tekniska högskolan.
2006 (engelsk)Inngår i: Journal of the American Chemical Society, ISSN 0002-7863, E-ISSN 1520-5126, Vol. 128, nr 10, s. 3414-3419Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

Synthesis of the heptasaccharyl myo-inositol found in Trypanosoma cruzi lipopeptidophosphoglycan was accomplished using a convergent assembly of three building blocks. The target compound is the first complete 2-aminoethyl phosphonic acid substituted glycan related to the glycosylphosphatidylinositol anchor family to be synthesized. The order of assembly enables synthesis of phosphoinositol oligosaccharides related to other glycosylinositolphospholipids in Tr. cruzi, the protozoan parasite causing Chagas' disease, which is endemic in South America.

sted, utgiver, år, opplag, sider
2006. Vol. 128, nr 10, s. 3414-3419
HSV kategori
Identifikatorer
URN: urn:nbn:se:liu:diva-50263DOI: 10.1021/ja057339bOAI: oai:DiVA.org:liu-50263DiVA, id: diva2:271159
Tilgjengelig fra: 2009-10-11 Laget: 2009-10-11 Sist oppdatert: 2017-12-12
Inngår i avhandling
1. Synthesis of inositolphosphoglycans found in Trypanosoma cruzi and development of novel carbohydrate monomolecular layers
Åpne denne publikasjonen i ny fane eller vindu >>Synthesis of inositolphosphoglycans found in Trypanosoma cruzi and development of novel carbohydrate monomolecular layers
2005 (engelsk)Doktoravhandling, med artikler (Annet vitenskapelig)
Abstract [en]

In this thesis, synthetic carbohydrate chemistry has been utilized to contribute to the fundamental understanding of three biological relevant areas. These include parasite cell-membrane glycoconjugates, protein-resistant surfaces and antifreeze glycoproteins.

The synthesis of inositolphosphoglycans found in Trypanosoma cruzi, the pathogen of Chagas´ disease, is described. A protected derivative of 6-(2-aminoethyl phosphonic acid)-2-amino-2-deoxy-α-D-glucopyranosyl-(1→6)-D-myo-inositol-1-phosphate was identified as an appropriate acceptor to give a synthetic route to the core oligosaccharide of T. cruzi glycoinositolphospholipids. The assembly of three building blocks accomplished the synthesis of the heptasaccharyl myo-inositol Galf(β1→3)-Manp(α1→2)-[Galf(β1→3)]-Manp(α1→2)-Manp(α1→6)-Manp(α1→4)-6-(2 -aminoethyl phosphonic acid)-GlcNp-(α1→6)-myo-Ins-1-PO4, the glycan of the T. cruzi lipopeptidophosphoglycan.

Carbohydrate self-assembled monolayers (SAMs) on gold were designed, synthesized and characterized to investigate their protein rejecting properties. Synthesis of methylated and non-methylated galactose-terminated alkanethiols provided mixed carbohydrate monomolecular layers. The physiochemical properties of the mixed SAMs were elucidated with ellipsometry, infrared reflection-absorption spectroscopy and contact angle goniometry. The irreversible adsorption of the model proteins fibrinogen and lysozyme was determined with ex-situ ellipsometry. Neither of the proteins adsorbed within a mixed regime corresponding to contact angles of water between 24° and 45°.

A carbohydrate model system mimicking the properties of antifreeze glycoproteins was developed. A Gal(β1→3)-GalNAc terminated 16-mercapto-hexadecanoic acid derivative was synthesized and co-adsorbed with an ethyl-terminated thiol in various proportions to form mixed SAMs on gold. The monolayers were characterized and the antifreeze model system was evaluated by initial ice nucleation studies.

Synthetic routes to protected ethyl 2-deoxy-2-phthalimido-1-β-D-thio-galactosamine derivatives via epimerization of corresponding glucosamine compounds were explored to provide methods in future synthesis of antifreeze glycoproteins and analogues.

sted, utgiver, år, opplag, sider
Linköping: Linköpings universitet, 2005. s. 63
Serie
Linköping Studies in Science and Technology. Dissertations, ISSN 0345-7524 ; 980
HSV kategori
Identifikatorer
urn:nbn:se:liu:diva-29937 (URN)15363 (Lokal ID)91-85457-56-6 (ISBN)15363 (Arkivnummer)15363 (OAI)
Disputas
2005-12-02, Planck, Fysikhuset, Campus Valla, Linköpings universitet, Linköping, 10:15 (engelsk)
Opponent
Tilgjengelig fra: 2009-10-09 Laget: 2009-10-09 Sist oppdatert: 2012-12-04bibliografisk kontrollert

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