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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...

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Autores principales: Ritchie, Gayle, Harvey, David J., Feldmann, Friederike, Stroeher, Ute, Feldmann, Heinz, Royle, Louise, Dwek, Raymond A., Rudd, Pauline M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Inc. 2010
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.
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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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