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
Autor(a) principal: | |
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Data de Publicação: | 1995 |
Outros Autores: | , , , , |
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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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 |
|
_version_ |
1802764151577116672 |