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 in | Molecules (Basel, Switzerland) Vol. 26; no. 18; p. 5652 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
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17.09.2021
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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). |
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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 – name: 3 Hokkaido Institute of Public Health, Sapporo 060-0819, Japan; yamano@iph.pref.hokkaido.jp |
Author_xml | – sequence: 1 givenname: Noriyasu surname: Hada fullname: Hada, Noriyasu – sequence: 2 givenname: Tokio orcidid: 0000-0001-5951-2981 surname: Morita fullname: Morita, Tokio – sequence: 3 givenname: Takashi orcidid: 0000-0002-4134-696X surname: Ueda fullname: Ueda, Takashi – sequence: 4 givenname: Kazuki surname: Masuda fullname: Masuda, Kazuki – sequence: 5 givenname: Hiromi surname: Nakane fullname: Nakane, Hiromi – sequence: 6 givenname: Mami surname: Ogane fullname: Ogane, Mami – sequence: 7 givenname: Kimiaki surname: Yamano fullname: Yamano, Kimiaki – sequence: 8 givenname: Frank orcidid: 0000-0001-8697-5519 surname: Schweizer fullname: Schweizer, Frank – sequence: 9 givenname: Fumiyuki orcidid: 0000-0002-9338-5047 surname: Kiuchi fullname: Kiuchi, Fumiyuki |
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Keywords | host-parasite interaction stereocontrolled synthesis glycoprotein biotin probe Echinococcus granulosus |
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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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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 https://www.proquest.com/docview/2576482399 https://www.proquest.com/docview/2577447751 https://pubmed.ncbi.nlm.nih.gov/PMC8468584 https://doaj.org/article/c904662f9a0b4652bf62c09eec187e66 |
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