Synthesis of the Carbohydrate Moiety of Glycoproteins from the Parasite Echinococcus granulosus and Their Antigenicity against Human Sera

Stereocontrolled syntheses of biotin-labeled oligosaccharide portions containing the carbohydrate moiety of glycoprotein from Echinococcus granulosus have been accomplished. Trisaccharide Galβ1-3Galβ1-3GalNAcα1-R (A), tetrasaccharide Galα1-4Galβ1-3Galβ1-3GalNAcα1-R (B), and pentasaccharide Galα1-4Ga...

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Published inMolecules (Basel, Switzerland) Vol. 26; no. 18; p. 5652
Main Authors Hada, Noriyasu, Morita, Tokio, Ueda, Takashi, Masuda, Kazuki, Nakane, Hiromi, Ogane, Mami, Yamano, Kimiaki, Schweizer, Frank, Kiuchi, Fumiyuki
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LanguageEnglish
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Abstract Stereocontrolled syntheses of biotin-labeled oligosaccharide portions containing the carbohydrate moiety of glycoprotein from Echinococcus granulosus have been accomplished. Trisaccharide Galβ1-3Galβ1-3GalNAcα1-R (A), tetrasaccharide Galα1-4Galβ1-3Galβ1-3GalNAcα1-R (B), and pentasaccharide Galα1-4Galβ1-3Galβ1-3Galβ1-3GalNAcα1-R (C), (R = biotinylated probe) were synthesized by stepwise condensation and/or block synthesis by the use of 5-(methoxycarbonyl)pentyl 2-azido-4,6-O-benzylidene-2-deoxy-α-d-galactopyranoside as a common glycosyl acceptor. The synthesis of the tetrasaccharide and the pentasaccharide was improved from the viewpoint of reducing the number of synthetic steps and increasing the total yield by changing from stepwise condensation to block synthesis. Moreover, hexasaccharide E, which contains the oligosaccharide sequence which occurs in E. granulosus, was synthesized from trisaccharide D. We examined the antigenicity of these five oligosaccharides by an enzyme-linked immunosorbent assay (ELISA). Although compounds of C–E did not exhibit antigenicity against cystic echinococcosis (CE) patient sera, compounds B, D, and E showed good serodiagnostic potential for alveolar echinococcosis (AE).
AbstractList Stereocontrolled syntheses of biotin-labeled oligosaccharide portions containing the carbohydrate moiety of glycoprotein from Echinococcus granulosus have been accomplished. Trisaccharide Galβ1-3Galβ1-3GalNAcα1-R ( A ), tetrasaccharide Galα1-4Galβ1-3Galβ1-3GalNAcα1-R ( B ), and pentasaccharide Galα1-4Galβ1-3Galβ1-3Galβ1-3GalNAcα1-R ( C ), (R = biotinylated probe) were synthesized by stepwise condensation and/or block synthesis by the use of 5-(methoxycarbonyl)pentyl 2-azido-4,6- O -benzylidene-2-deoxy-α- d -galactopyranoside as a common glycosyl acceptor. The synthesis of the tetrasaccharide and the pentasaccharide was improved from the viewpoint of reducing the number of synthetic steps and increasing the total yield by changing from stepwise condensation to block synthesis. Moreover, hexasaccharide E , which contains the oligosaccharide sequence which occurs in E. granulosus , was synthesized from trisaccharide D . We examined the antigenicity of these five oligosaccharides by an enzyme-linked immunosorbent assay (ELISA). Although compounds of C – E did not exhibit antigenicity against cystic echinococcosis (CE) patient sera, compounds B , D , and E showed good serodiagnostic potential for alveolar echinococcosis (AE).
Stereocontrolled syntheses of biotin-labeled oligosaccharide portions containing the carbohydrate moiety of glycoprotein from Echinococcus granulosus have been accomplished. Trisaccharide Galβ1-3Galβ1-3GalNAcα1-R (A), tetrasaccharide Galα1-4Galβ1-3Galβ1-3GalNAcα1-R (B), and pentasaccharide Galα1-4Galβ1-3Galβ1-3Galβ1-3GalNAcα1-R (C), (R = biotinylated probe) were synthesized by stepwise condensation and/or block synthesis by the use of 5-(methoxycarbonyl)pentyl 2-azido-4,6-O-benzylidene-2-deoxy-α-d-galactopyranoside as a common glycosyl acceptor. The synthesis of the tetrasaccharide and the pentasaccharide was improved from the viewpoint of reducing the number of synthetic steps and increasing the total yield by changing from stepwise condensation to block synthesis. Moreover, hexasaccharide E, which contains the oligosaccharide sequence which occurs in E. granulosus, was synthesized from trisaccharide D. We examined the antigenicity of these five oligosaccharides by an enzyme-linked immunosorbent assay (ELISA). Although compounds of C-E did not exhibit antigenicity against cystic echinococcosis (CE) patient sera, compounds B, D, and E showed good serodiagnostic potential for alveolar echinococcosis (AE).Stereocontrolled syntheses of biotin-labeled oligosaccharide portions containing the carbohydrate moiety of glycoprotein from Echinococcus granulosus have been accomplished. Trisaccharide Galβ1-3Galβ1-3GalNAcα1-R (A), tetrasaccharide Galα1-4Galβ1-3Galβ1-3GalNAcα1-R (B), and pentasaccharide Galα1-4Galβ1-3Galβ1-3Galβ1-3GalNAcα1-R (C), (R = biotinylated probe) were synthesized by stepwise condensation and/or block synthesis by the use of 5-(methoxycarbonyl)pentyl 2-azido-4,6-O-benzylidene-2-deoxy-α-d-galactopyranoside as a common glycosyl acceptor. The synthesis of the tetrasaccharide and the pentasaccharide was improved from the viewpoint of reducing the number of synthetic steps and increasing the total yield by changing from stepwise condensation to block synthesis. Moreover, hexasaccharide E, which contains the oligosaccharide sequence which occurs in E. granulosus, was synthesized from trisaccharide D. We examined the antigenicity of these five oligosaccharides by an enzyme-linked immunosorbent assay (ELISA). Although compounds of C-E did not exhibit antigenicity against cystic echinococcosis (CE) patient sera, compounds B, D, and E showed good serodiagnostic potential for alveolar echinococcosis (AE).
Stereocontrolled syntheses of biotin-labeled oligosaccharide portions containing the carbohydrate moiety of glycoprotein from Echinococcus granulosus have been accomplished. Trisaccharide Galβ1-3Galβ1-3GalNAcα1-R (A), tetrasaccharide Galα1-4Galβ1-3Galβ1-3GalNAcα1-R (B), and pentasaccharide Galα1-4Galβ1-3Galβ1-3Galβ1-3GalNAcα1-R (C), (R = biotinylated probe) were synthesized by stepwise condensation and/or block synthesis by the use of 5-(methoxycarbonyl)pentyl 2-azido-4,6-O-benzylidene-2-deoxy-α-d-galactopyranoside as a common glycosyl acceptor. The synthesis of the tetrasaccharide and the pentasaccharide was improved from the viewpoint of reducing the number of synthetic steps and increasing the total yield by changing from stepwise condensation to block synthesis. Moreover, hexasaccharide E, which contains the oligosaccharide sequence which occurs in E. granulosus, was synthesized from trisaccharide D. We examined the antigenicity of these five oligosaccharides by an enzyme-linked immunosorbent assay (ELISA). Although compounds of C–E did not exhibit antigenicity against cystic echinococcosis (CE) patient sera, compounds B, D, and E showed good serodiagnostic potential for alveolar echinococcosis (AE).
Stereocontrolled syntheses of biotin-labeled oligosaccharide portions containing the carbohydrate moiety of glycoprotein from have been accomplished. Trisaccharide Galβ1-3Galβ1-3GalNAcα1-R ( ), tetrasaccharide Galα1-4Galβ1-3Galβ1-3GalNAcα1-R ( ), and pentasaccharide Galα1-4Galβ1-3Galβ1-3Galβ1-3GalNAcα1-R ( ), (R = biotinylated probe) were synthesized by stepwise condensation and/or block synthesis by the use of 5-(methoxycarbonyl)pentyl 2-azido-4,6- -benzylidene-2-deoxy-α-d-galactopyranoside as a common glycosyl acceptor. The synthesis of the tetrasaccharide and the pentasaccharide was improved from the viewpoint of reducing the number of synthetic steps and increasing the total yield by changing from stepwise condensation to block synthesis. Moreover, hexasaccharide , which contains the oligosaccharide sequence which occurs in , was synthesized from trisaccharide . We examined the antigenicity of these five oligosaccharides by an enzyme-linked immunosorbent assay (ELISA). Although compounds of - did not exhibit antigenicity against cystic echinococcosis (CE) patient sera, compounds , , and showed good serodiagnostic potential for alveolar echinococcosis (AE).
Author Morita, Tokio
Kiuchi, Fumiyuki
Masuda, Kazuki
Ogane, Mami
Yamano, Kimiaki
Schweizer, Frank
Nakane, Hiromi
Hada, Noriyasu
Ueda, Takashi
AuthorAffiliation 4 Department of Chemistry and Biochemistry, Faculty of Science, University of Manitoba, Winnipeg, MB R3T 2N2, Canada; Frank.Schweizer@umanitoba.ca
2 Faculty of Pharmacy, Keio University, Tokyo 105-8512, Japan; morita.tokio@keio.jp (T.M.); zacro.ueda@gmail.com (T.U.); masudakazuki0000@gmail.com (K.M.); beautifulocean.june@gmail.com (H.N.); mamium-07@hotmail.co.jp (M.O.); kiuchi-fm84@keio.jp (F.K.)
3 Hokkaido Institute of Public Health, Sapporo 060-0819, Japan; yamano@iph.pref.hokkaido.jp
1 Faculty of Pharmaceutical Sciences, Tokyo University of Science, Chiba 278-8510, Japan
AuthorAffiliation_xml – name: 2 Faculty of Pharmacy, Keio University, Tokyo 105-8512, Japan; morita.tokio@keio.jp (T.M.); zacro.ueda@gmail.com (T.U.); masudakazuki0000@gmail.com (K.M.); beautifulocean.june@gmail.com (H.N.); mamium-07@hotmail.co.jp (M.O.); kiuchi-fm84@keio.jp (F.K.)
– name: 4 Department of Chemistry and Biochemistry, Faculty of Science, University of Manitoba, Winnipeg, MB R3T 2N2, Canada; Frank.Schweizer@umanitoba.ca
– name: 1 Faculty of Pharmaceutical Sciences, Tokyo University of Science, Chiba 278-8510, Japan
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Keywords host-parasite interaction
stereocontrolled synthesis
glycoprotein
biotin probe
Echinococcus granulosus
Language English
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Snippet Stereocontrolled syntheses of biotin-labeled oligosaccharide portions containing the carbohydrate moiety of glycoprotein from Echinococcus granulosus have been...
Stereocontrolled syntheses of biotin-labeled oligosaccharide portions containing the carbohydrate moiety of glycoprotein from have been accomplished....
Stereocontrolled syntheses of biotin-labeled oligosaccharide portions containing the carbohydrate moiety of glycoprotein from Echinococcus granulosus have been...
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StartPage 5652
SubjectTerms Animals
Antigens
Antigens, Helminth - immunology
biotin probe
Carbohydrates
Carbohydrates - biosynthesis
Carbohydrates - chemistry
Chromatography
Echinococcus granulosus
Echinococcus granulosus - metabolism
Enzyme-Linked Immunosorbent Assay
glycoprotein
Glycoproteins
Glycoproteins - chemistry
host-parasite interaction
Humans
Parasites
Parasites - metabolism
Parasitic diseases
Serum - immunology
Spectrum analysis
stereocontrolled synthesis
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Title Synthesis of the Carbohydrate Moiety of Glycoproteins from the Parasite Echinococcus granulosus and Their Antigenicity against Human Sera
URI https://www.ncbi.nlm.nih.gov/pubmed/34577122
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Volume 26
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