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Identification of N-linked carbohydrates from severe acute respiratory syndrome (SARS) spike glycoprotein
N-glycans were released from the SARS coronavirus (SARS-CoV) spike glycoprotein produced in Vero E6 cells and their structures were determined by a combination of matrix-assisted laser desorption/ionization (MALDI) mass spectrometry, negative ion electrospray collision-induced dissociation time-of-f...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Inc.
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3412594/ https://www.ncbi.nlm.nih.gov/pubmed/20129637 http://dx.doi.org/10.1016/j.virol.2009.12.020 |
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author | Ritchie, Gayle Harvey, David J. Feldmann, Friederike Stroeher, Ute Feldmann, Heinz Royle, Louise Dwek, Raymond A. Rudd, Pauline M. |
author_facet | Ritchie, Gayle Harvey, David J. Feldmann, Friederike Stroeher, Ute Feldmann, Heinz Royle, Louise Dwek, Raymond A. Rudd, Pauline M. |
author_sort | Ritchie, Gayle |
collection | PubMed |
description | N-glycans were released from the SARS coronavirus (SARS-CoV) spike glycoprotein produced in Vero E6 cells and their structures were determined by a combination of matrix-assisted laser desorption/ionization (MALDI) mass spectrometry, negative ion electrospray collision-induced dissociation time-of-flight mass spectrometry and normal-phase high-performance liquid chromatography with exoglycosidase digestion. Major glycans were high-mannose (Man(5–9)GlcNAc(2)), hybrid and bi-, tri- and tetra-antennary complex with and without bisecting GlcNAc and core fucose. Complex glycans with fewer than the full complement of galactose residues were present and sialylation was negligible. Treatment with the glucosidase inhibitor N-butyl-deoxynojirimycin (NB-DNJ) inhibited N-glycan processing as evidenced by the appearance of glycans of composition Glc(3)Man(7–9)GlcNAc(2). However, some complex glycans remained suggesting the presence of an α-endomannosidase. Our data in tissue culture indicate that inhibition of N-glycan processing may be considered as a therapeutic strategy against SARS CoV infections. |
format | Online Article Text |
id | pubmed-3412594 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Elsevier Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-34125942012-08-06 Identification of N-linked carbohydrates from severe acute respiratory syndrome (SARS) spike glycoprotein Ritchie, Gayle Harvey, David J. Feldmann, Friederike Stroeher, Ute Feldmann, Heinz Royle, Louise Dwek, Raymond A. Rudd, Pauline M. Virology Article N-glycans were released from the SARS coronavirus (SARS-CoV) spike glycoprotein produced in Vero E6 cells and their structures were determined by a combination of matrix-assisted laser desorption/ionization (MALDI) mass spectrometry, negative ion electrospray collision-induced dissociation time-of-flight mass spectrometry and normal-phase high-performance liquid chromatography with exoglycosidase digestion. Major glycans were high-mannose (Man(5–9)GlcNAc(2)), hybrid and bi-, tri- and tetra-antennary complex with and without bisecting GlcNAc and core fucose. Complex glycans with fewer than the full complement of galactose residues were present and sialylation was negligible. Treatment with the glucosidase inhibitor N-butyl-deoxynojirimycin (NB-DNJ) inhibited N-glycan processing as evidenced by the appearance of glycans of composition Glc(3)Man(7–9)GlcNAc(2). However, some complex glycans remained suggesting the presence of an α-endomannosidase. Our data in tissue culture indicate that inhibition of N-glycan processing may be considered as a therapeutic strategy against SARS CoV infections. Elsevier Inc. 2010-04-10 2010-02-02 /pmc/articles/PMC3412594/ /pubmed/20129637 http://dx.doi.org/10.1016/j.virol.2009.12.020 Text en Copyright © 2009 Elsevier Inc. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Ritchie, Gayle Harvey, David J. Feldmann, Friederike Stroeher, Ute Feldmann, Heinz Royle, Louise Dwek, Raymond A. Rudd, Pauline M. Identification of N-linked carbohydrates from severe acute respiratory syndrome (SARS) spike glycoprotein |
title | Identification of N-linked carbohydrates from severe acute respiratory syndrome (SARS) spike glycoprotein |
title_full | Identification of N-linked carbohydrates from severe acute respiratory syndrome (SARS) spike glycoprotein |
title_fullStr | Identification of N-linked carbohydrates from severe acute respiratory syndrome (SARS) spike glycoprotein |
title_full_unstemmed | Identification of N-linked carbohydrates from severe acute respiratory syndrome (SARS) spike glycoprotein |
title_short | Identification of N-linked carbohydrates from severe acute respiratory syndrome (SARS) spike glycoprotein |
title_sort | identification of n-linked carbohydrates from severe acute respiratory syndrome (sars) spike glycoprotein |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3412594/ https://www.ncbi.nlm.nih.gov/pubmed/20129637 http://dx.doi.org/10.1016/j.virol.2009.12.020 |
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