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Characterization of sheep erythrocyte glycosphingolipids recognized by human anti-Forssman antibodies

The FORS histo-blood group system is the most recently discovered carbohydrate-based human blood group system. FORS is a rare blood group system, and most individuals have naturally occurring anti-FORS1 antibodies in plasma. Screening for anti-FORS1 antibodies is often done by hemagglutination assay...

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Autores principales: Santos, Licinia, Jin, Chunsheng, Mourato, Cristiana, Mendes, Fernando, Hesse, Camilla, Teneberg, Susann
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7581655/
https://www.ncbi.nlm.nih.gov/pubmed/32280958
http://dx.doi.org/10.1093/glycob/cwaa032
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author Santos, Licinia
Jin, Chunsheng
Mourato, Cristiana
Mendes, Fernando
Hesse, Camilla
Teneberg, Susann
author_facet Santos, Licinia
Jin, Chunsheng
Mourato, Cristiana
Mendes, Fernando
Hesse, Camilla
Teneberg, Susann
author_sort Santos, Licinia
collection PubMed
description The FORS histo-blood group system is the most recently discovered carbohydrate-based human blood group system. FORS is a rare blood group system, and most individuals have naturally occurring anti-FORS1 antibodies in plasma. Screening for anti-FORS1 antibodies is often done by hemagglutination assays using FORS1-expressing sheep erythrocytes, since FORS1-positive human erythrocytes are most often not available. Here, we have characterized the non-acid glycosphingolipids from sheep erythrocytes and isolated subfractions, with mass spectrometry, binding of antibodies and lectins, and by enzymatic hydrolysis. This demonstrated the presence of Forssman and Galili pentaosylceramides, and a Galili heptaosylceramide. Two complex glycosphingolipids recognized by human anti-FORS1 antibodies were characterized as a Forssman neolacto hybrid hexaosylceramide (GalNAcα3GalNAcβ3Galβ4GlcNAcβ3Galβ4Glcβ1Cer) and a Forssman Galili hybrid heptaosylceramide (GalNAcα3GalNAcβ3Galα3Galβ4GlcNAcβ3Galβ4Glcβ1Cer). These are novel glycosphingolipid structures, and to our knowledge, the first case of an elongated Galili antigen. Thus, the anti-Forssman antibodies in human serum bind not only to the classical Forssman pentaosylceramide (GalNAcα3GalNAcβ3Galα4Galβ4Glcβ1Cer), but also when the GalNAcα3GalNAcβ3 sequence is presented on a neolacto core chain and even on a Galili carbohydrate sequence.
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spelling pubmed-75816552020-10-29 Characterization of sheep erythrocyte glycosphingolipids recognized by human anti-Forssman antibodies Santos, Licinia Jin, Chunsheng Mourato, Cristiana Mendes, Fernando Hesse, Camilla Teneberg, Susann Glycobiology Glycan Recognition The FORS histo-blood group system is the most recently discovered carbohydrate-based human blood group system. FORS is a rare blood group system, and most individuals have naturally occurring anti-FORS1 antibodies in plasma. Screening for anti-FORS1 antibodies is often done by hemagglutination assays using FORS1-expressing sheep erythrocytes, since FORS1-positive human erythrocytes are most often not available. Here, we have characterized the non-acid glycosphingolipids from sheep erythrocytes and isolated subfractions, with mass spectrometry, binding of antibodies and lectins, and by enzymatic hydrolysis. This demonstrated the presence of Forssman and Galili pentaosylceramides, and a Galili heptaosylceramide. Two complex glycosphingolipids recognized by human anti-FORS1 antibodies were characterized as a Forssman neolacto hybrid hexaosylceramide (GalNAcα3GalNAcβ3Galβ4GlcNAcβ3Galβ4Glcβ1Cer) and a Forssman Galili hybrid heptaosylceramide (GalNAcα3GalNAcβ3Galα3Galβ4GlcNAcβ3Galβ4Glcβ1Cer). These are novel glycosphingolipid structures, and to our knowledge, the first case of an elongated Galili antigen. Thus, the anti-Forssman antibodies in human serum bind not only to the classical Forssman pentaosylceramide (GalNAcα3GalNAcβ3Galα4Galβ4Glcβ1Cer), but also when the GalNAcα3GalNAcβ3 sequence is presented on a neolacto core chain and even on a Galili carbohydrate sequence. Oxford University Press 2020-04-13 /pmc/articles/PMC7581655/ /pubmed/32280958 http://dx.doi.org/10.1093/glycob/cwaa032 Text en © The Author(s) 2020. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Glycan Recognition
Santos, Licinia
Jin, Chunsheng
Mourato, Cristiana
Mendes, Fernando
Hesse, Camilla
Teneberg, Susann
Characterization of sheep erythrocyte glycosphingolipids recognized by human anti-Forssman antibodies
title Characterization of sheep erythrocyte glycosphingolipids recognized by human anti-Forssman antibodies
title_full Characterization of sheep erythrocyte glycosphingolipids recognized by human anti-Forssman antibodies
title_fullStr Characterization of sheep erythrocyte glycosphingolipids recognized by human anti-Forssman antibodies
title_full_unstemmed Characterization of sheep erythrocyte glycosphingolipids recognized by human anti-Forssman antibodies
title_short Characterization of sheep erythrocyte glycosphingolipids recognized by human anti-Forssman antibodies
title_sort characterization of sheep erythrocyte glycosphingolipids recognized by human anti-forssman antibodies
topic Glycan Recognition
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7581655/
https://www.ncbi.nlm.nih.gov/pubmed/32280958
http://dx.doi.org/10.1093/glycob/cwaa032
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