THE LIPID STRUCTURE OF THE GLYCOSYLPHOSPHATIDYLINOSITOL-ANCHORED MUCIN-LIKE SIALIC-ACID ACCEPTORS OF TRYPANOSOMA-CRUZI CHANGES DURING PARASITE DIFFERENTIATION FROM EPIMASTIGOTES TO INFECTIVE METACYCLIC TRYPOMASTIGOTE FORMS

Detalhes bibliográficos
Autor(a) principal: Serrano, Alvaro Acosta [UNIFESP]
Data de Publicação: 1995
Outros Autores: Schenkman, Sergio [UNIFESP], Yoshida, Nobuko [UNIFESP], Mehlert, A., Richardson, J. M., Ferguson, MAJ
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://repositorio.unifesp.br/11600/44204
http://doi.org/10.1074/jbc.270.45.27244
Resumo: The major accepters of sialic acid on the surface of metacyclic trypomastigotes, which are the infective forms of Trypanosoma cruzi found in the insect vector, are mucin-like glycoproteins linked to the parasite membrane via glycosylphosphatidylinositol anchors. Here we have compared the lipid and the carbohydrate structure of the glycosylphosphatidylinositol anchors and the O-linked oligosaccharides of the mucins isolated from metacyclic trypomastigotes and noninfective epimastigote forms obtained in culture. The single difference found was in the lipid structure. While the phosphatidylinositol moiety of the epimastigote mucins contains mainly 1-O-hexadecyl-2-O-hexadecanoylphos phatidylinositol, the phosphatidylinositol moiety of the metacyclic trypomastigote mucins contains mostly (similar to 70%) inositol phosphoceramides, consisting of a C-18:0 sphinganine long chain base and mainly C-24:0 and C-16:0 fatty acids. The remaining 30% of the metacyclic phosphatidylinositol moieties are the same alkylacylphosphatidylinositol species found in epimastigotes. In contrast, the glycosylphosphatidylinositol glycan cores of both molecules are very similar, mainly Man alpha 1-2Man alpha 1-2Man alpha 1-6Man alpha 1-4GlcN. The glycans are substituted at the GlcN residue and at the third alpha Man distal to the GlcN residue by ethanolamine phosphate or 2-aminoethylphosphonate groups. The structures of the desialylated O-linked oligosaccharides of the metacyclic trypomastigote mucin-like molecules, released by beta-elimination with concomitant reduction, are identical to the structures reported for the epimastigote mucins (Previato, J. O., Jones, C., Goncalves, L. P. B., Wait, R., Travassos, L, R., and Mendoca-Previato, L, (1994) Biochem. J. 301, 151-159), In addition, a significant amount of nonsubstituted N-acetylglucosaminitol was released from the mucins of both forms of the parasite, Taken together, these results indicate that when epimastigotes transform into infective metacyclic trypomastigotes, the phosphatidylinositol moiety of the glycosylphosphatidylinositol anchor of the major acceptor of sialic acid is modified, while the glycosylphosphatidylinositol anchor and O-linked sugar chains remain essentially unchanged.
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spelling Serrano, Alvaro Acosta [UNIFESP]Schenkman, Sergio [UNIFESP]Yoshida, Nobuko [UNIFESP]Mehlert, A.Richardson, J. M.Ferguson, MAJUNIV DUNDEEUniversidade Federal de São Paulo (UNIFESP)2018-06-15T17:53:05Z2018-06-15T17:53:05Z1995-11-10Journal Of Biological Chemistry. Bethesda: Amer Soc Biochemistry Molecular Biology Inc, v. 270, n. 45, p. 27244-27253, 1995.0021-9258http://repositorio.unifesp.br/11600/44204http://doi.org/10.1074/jbc.270.45.2724410.1074/jbc.270.45.27244WOS:A1995TE58300083The major accepters of sialic acid on the surface of metacyclic trypomastigotes, which are the infective forms of Trypanosoma cruzi found in the insect vector, are mucin-like glycoproteins linked to the parasite membrane via glycosylphosphatidylinositol anchors. Here we have compared the lipid and the carbohydrate structure of the glycosylphosphatidylinositol anchors and the O-linked oligosaccharides of the mucins isolated from metacyclic trypomastigotes and noninfective epimastigote forms obtained in culture. The single difference found was in the lipid structure. While the phosphatidylinositol moiety of the epimastigote mucins contains mainly 1-O-hexadecyl-2-O-hexadecanoylphos phatidylinositol, the phosphatidylinositol moiety of the metacyclic trypomastigote mucins contains mostly (similar to 70%) inositol phosphoceramides, consisting of a C-18:0 sphinganine long chain base and mainly C-24:0 and C-16:0 fatty acids. The remaining 30% of the metacyclic phosphatidylinositol moieties are the same alkylacylphosphatidylinositol species found in epimastigotes. In contrast, the glycosylphosphatidylinositol glycan cores of both molecules are very similar, mainly Man alpha 1-2Man alpha 1-2Man alpha 1-6Man alpha 1-4GlcN. The glycans are substituted at the GlcN residue and at the third alpha Man distal to the GlcN residue by ethanolamine phosphate or 2-aminoethylphosphonate groups. The structures of the desialylated O-linked oligosaccharides of the metacyclic trypomastigote mucin-like molecules, released by beta-elimination with concomitant reduction, are identical to the structures reported for the epimastigote mucins (Previato, J. O., Jones, C., Goncalves, L. P. B., Wait, R., Travassos, L, R., and Mendoca-Previato, L, (1994) Biochem. J. 301, 151-159), In addition, a significant amount of nonsubstituted N-acetylglucosaminitol was released from the mucins of both forms of the parasite, Taken together, these results indicate that when epimastigotes transform into infective metacyclic trypomastigotes, the phosphatidylinositol moiety of the glycosylphosphatidylinositol anchor of the major acceptor of sialic acid is modified, while the glycosylphosphatidylinositol anchor and O-linked sugar chains remain essentially unchanged.UNIV DUNDEE,DEPT BIOCHEM,DUNDEE DD1 4HN,SCOTLANDWeb of Science27244-27253engAmer Soc Biochemistry Molecular Biology IncJournal Of Biological ChemistryTHE LIPID STRUCTURE OF THE GLYCOSYLPHOSPHATIDYLINOSITOL-ANCHORED MUCIN-LIKE SIALIC-ACID ACCEPTORS OF TRYPANOSOMA-CRUZI CHANGES DURING PARASITE DIFFERENTIATION FROM EPIMASTIGOTES TO INFECTIVE METACYCLIC TRYPOMASTIGOTE FORMSinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP11600/442042021-10-05 21:55:28.391metadata only accessoai:repositorio.unifesp.br:11600/44204Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestopendoar:34652021-10-06T00:55:28Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.en.fl_str_mv THE LIPID STRUCTURE OF THE GLYCOSYLPHOSPHATIDYLINOSITOL-ANCHORED MUCIN-LIKE SIALIC-ACID ACCEPTORS OF TRYPANOSOMA-CRUZI CHANGES DURING PARASITE DIFFERENTIATION FROM EPIMASTIGOTES TO INFECTIVE METACYCLIC TRYPOMASTIGOTE FORMS
title THE LIPID STRUCTURE OF THE GLYCOSYLPHOSPHATIDYLINOSITOL-ANCHORED MUCIN-LIKE SIALIC-ACID ACCEPTORS OF TRYPANOSOMA-CRUZI CHANGES DURING PARASITE DIFFERENTIATION FROM EPIMASTIGOTES TO INFECTIVE METACYCLIC TRYPOMASTIGOTE FORMS
spellingShingle THE LIPID STRUCTURE OF THE GLYCOSYLPHOSPHATIDYLINOSITOL-ANCHORED MUCIN-LIKE SIALIC-ACID ACCEPTORS OF TRYPANOSOMA-CRUZI CHANGES DURING PARASITE DIFFERENTIATION FROM EPIMASTIGOTES TO INFECTIVE METACYCLIC TRYPOMASTIGOTE FORMS
Serrano, Alvaro Acosta [UNIFESP]
title_short THE LIPID STRUCTURE OF THE GLYCOSYLPHOSPHATIDYLINOSITOL-ANCHORED MUCIN-LIKE SIALIC-ACID ACCEPTORS OF TRYPANOSOMA-CRUZI CHANGES DURING PARASITE DIFFERENTIATION FROM EPIMASTIGOTES TO INFECTIVE METACYCLIC TRYPOMASTIGOTE FORMS
title_full THE LIPID STRUCTURE OF THE GLYCOSYLPHOSPHATIDYLINOSITOL-ANCHORED MUCIN-LIKE SIALIC-ACID ACCEPTORS OF TRYPANOSOMA-CRUZI CHANGES DURING PARASITE DIFFERENTIATION FROM EPIMASTIGOTES TO INFECTIVE METACYCLIC TRYPOMASTIGOTE FORMS
title_fullStr THE LIPID STRUCTURE OF THE GLYCOSYLPHOSPHATIDYLINOSITOL-ANCHORED MUCIN-LIKE SIALIC-ACID ACCEPTORS OF TRYPANOSOMA-CRUZI CHANGES DURING PARASITE DIFFERENTIATION FROM EPIMASTIGOTES TO INFECTIVE METACYCLIC TRYPOMASTIGOTE FORMS
title_full_unstemmed THE LIPID STRUCTURE OF THE GLYCOSYLPHOSPHATIDYLINOSITOL-ANCHORED MUCIN-LIKE SIALIC-ACID ACCEPTORS OF TRYPANOSOMA-CRUZI CHANGES DURING PARASITE DIFFERENTIATION FROM EPIMASTIGOTES TO INFECTIVE METACYCLIC TRYPOMASTIGOTE FORMS
title_sort THE LIPID STRUCTURE OF THE GLYCOSYLPHOSPHATIDYLINOSITOL-ANCHORED MUCIN-LIKE SIALIC-ACID ACCEPTORS OF TRYPANOSOMA-CRUZI CHANGES DURING PARASITE DIFFERENTIATION FROM EPIMASTIGOTES TO INFECTIVE METACYCLIC TRYPOMASTIGOTE FORMS
author Serrano, Alvaro Acosta [UNIFESP]
author_facet Serrano, Alvaro Acosta [UNIFESP]
Schenkman, Sergio [UNIFESP]
Yoshida, Nobuko [UNIFESP]
Mehlert, A.
Richardson, J. M.
Ferguson, MAJ
author_role author
author2 Schenkman, Sergio [UNIFESP]
Yoshida, Nobuko [UNIFESP]
Mehlert, A.
Richardson, J. M.
Ferguson, MAJ
author2_role author
author
author
author
author
dc.contributor.institution.none.fl_str_mv UNIV DUNDEE
Universidade Federal de São Paulo (UNIFESP)
dc.contributor.author.fl_str_mv Serrano, Alvaro Acosta [UNIFESP]
Schenkman, Sergio [UNIFESP]
Yoshida, Nobuko [UNIFESP]
Mehlert, A.
Richardson, J. M.
Ferguson, MAJ
description The major accepters of sialic acid on the surface of metacyclic trypomastigotes, which are the infective forms of Trypanosoma cruzi found in the insect vector, are mucin-like glycoproteins linked to the parasite membrane via glycosylphosphatidylinositol anchors. Here we have compared the lipid and the carbohydrate structure of the glycosylphosphatidylinositol anchors and the O-linked oligosaccharides of the mucins isolated from metacyclic trypomastigotes and noninfective epimastigote forms obtained in culture. The single difference found was in the lipid structure. While the phosphatidylinositol moiety of the epimastigote mucins contains mainly 1-O-hexadecyl-2-O-hexadecanoylphos phatidylinositol, the phosphatidylinositol moiety of the metacyclic trypomastigote mucins contains mostly (similar to 70%) inositol phosphoceramides, consisting of a C-18:0 sphinganine long chain base and mainly C-24:0 and C-16:0 fatty acids. The remaining 30% of the metacyclic phosphatidylinositol moieties are the same alkylacylphosphatidylinositol species found in epimastigotes. In contrast, the glycosylphosphatidylinositol glycan cores of both molecules are very similar, mainly Man alpha 1-2Man alpha 1-2Man alpha 1-6Man alpha 1-4GlcN. The glycans are substituted at the GlcN residue and at the third alpha Man distal to the GlcN residue by ethanolamine phosphate or 2-aminoethylphosphonate groups. The structures of the desialylated O-linked oligosaccharides of the metacyclic trypomastigote mucin-like molecules, released by beta-elimination with concomitant reduction, are identical to the structures reported for the epimastigote mucins (Previato, J. O., Jones, C., Goncalves, L. P. B., Wait, R., Travassos, L, R., and Mendoca-Previato, L, (1994) Biochem. J. 301, 151-159), In addition, a significant amount of nonsubstituted N-acetylglucosaminitol was released from the mucins of both forms of the parasite, Taken together, these results indicate that when epimastigotes transform into infective metacyclic trypomastigotes, the phosphatidylinositol moiety of the glycosylphosphatidylinositol anchor of the major acceptor of sialic acid is modified, while the glycosylphosphatidylinositol anchor and O-linked sugar chains remain essentially unchanged.
publishDate 1995
dc.date.issued.fl_str_mv 1995-11-10
dc.date.accessioned.fl_str_mv 2018-06-15T17:53:05Z
dc.date.available.fl_str_mv 2018-06-15T17:53:05Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.citation.fl_str_mv Journal Of Biological Chemistry. Bethesda: Amer Soc Biochemistry Molecular Biology Inc, v. 270, n. 45, p. 27244-27253, 1995.
dc.identifier.uri.fl_str_mv http://repositorio.unifesp.br/11600/44204
http://doi.org/10.1074/jbc.270.45.27244
dc.identifier.issn.none.fl_str_mv 0021-9258
dc.identifier.doi.none.fl_str_mv 10.1074/jbc.270.45.27244
dc.identifier.wos.none.fl_str_mv WOS:A1995TE58300083
identifier_str_mv Journal Of Biological Chemistry. Bethesda: Amer Soc Biochemistry Molecular Biology Inc, v. 270, n. 45, p. 27244-27253, 1995.
0021-9258
10.1074/jbc.270.45.27244
WOS:A1995TE58300083
url http://repositorio.unifesp.br/11600/44204
http://doi.org/10.1074/jbc.270.45.27244
dc.language.iso.fl_str_mv eng
language eng
dc.relation.ispartof.none.fl_str_mv Journal Of Biological Chemistry
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 27244-27253
dc.publisher.none.fl_str_mv Amer Soc Biochemistry Molecular Biology Inc
publisher.none.fl_str_mv Amer Soc Biochemistry Molecular Biology Inc
dc.source.none.fl_str_mv reponame:Repositório Institucional da UNIFESP
instname:Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
instname_str Universidade Federal de São Paulo (UNIFESP)
instacron_str UNIFESP
institution UNIFESP
reponame_str Repositório Institucional da UNIFESP
collection Repositório Institucional da UNIFESP
repository.name.fl_str_mv Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)
repository.mail.fl_str_mv
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