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The opportunity cost of automated glycopeptide analysis: case study profiling the SARS-CoV-2 S glycoprotein
Glycosylation analysis of viral glycoproteins contributes significantly to vaccine design and development. Among other benefits, glycosylation analysis allows vaccine developers to assess the impact of construct design or producer cell line choices for vaccine production, and it is a key measure by...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8390178/ https://www.ncbi.nlm.nih.gov/pubmed/34448030 http://dx.doi.org/10.1007/s00216-021-03621-z |
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author | Go, Eden P. Zhang, Shijian Ding, Haitao Kappes, John C. Sodroski, Joseph Desaire, Heather |
author_facet | Go, Eden P. Zhang, Shijian Ding, Haitao Kappes, John C. Sodroski, Joseph Desaire, Heather |
author_sort | Go, Eden P. |
collection | PubMed |
description | Glycosylation analysis of viral glycoproteins contributes significantly to vaccine design and development. Among other benefits, glycosylation analysis allows vaccine developers to assess the impact of construct design or producer cell line choices for vaccine production, and it is a key measure by which glycoproteins that are produced for use in vaccination can be compared to their native viral forms. Because many viral glycoproteins are multiply glycosylated, glycopeptide analysis is a preferrable approach for mapping the glycans, yet the analysis of glycopeptide data can be cumbersome and requires the expertise of an experienced analyst. In recent years, a commercial software product, Byonic, has been implemented in several instances to facilitate glycopeptide analysis on viral glycoproteins and other glycoproteomics data sets, and the purpose of the study herein is to determine the strengths and limitations of using this software, particularly in cases relevant to vaccine development. The glycopeptides from a recombinantly expressed trimeric S glycoprotein of the SARS-CoV-2 virus were first analyzed using an expert-based analysis strategy; subsequently, analysis of the same data set was completed using Byonic. Careful assessment of instances where the two methods produced different results revealed that the glycopeptide assignments from Byonic contained more false positives than true positives, even when the data were assessed using a 1% false discovery rate. The work herein provides a roadmap for removing the spurious assignments that Byonic generates, and it provides an assessment of the opportunity cost for relying on automated assignments for glycopeptide data sets from viral glycoproteins. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00216-021-03621-z. |
format | Online Article Text |
id | pubmed-8390178 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-83901782021-08-27 The opportunity cost of automated glycopeptide analysis: case study profiling the SARS-CoV-2 S glycoprotein Go, Eden P. Zhang, Shijian Ding, Haitao Kappes, John C. Sodroski, Joseph Desaire, Heather Anal Bioanal Chem Paper in Forefront Glycosylation analysis of viral glycoproteins contributes significantly to vaccine design and development. Among other benefits, glycosylation analysis allows vaccine developers to assess the impact of construct design or producer cell line choices for vaccine production, and it is a key measure by which glycoproteins that are produced for use in vaccination can be compared to their native viral forms. Because many viral glycoproteins are multiply glycosylated, glycopeptide analysis is a preferrable approach for mapping the glycans, yet the analysis of glycopeptide data can be cumbersome and requires the expertise of an experienced analyst. In recent years, a commercial software product, Byonic, has been implemented in several instances to facilitate glycopeptide analysis on viral glycoproteins and other glycoproteomics data sets, and the purpose of the study herein is to determine the strengths and limitations of using this software, particularly in cases relevant to vaccine development. The glycopeptides from a recombinantly expressed trimeric S glycoprotein of the SARS-CoV-2 virus were first analyzed using an expert-based analysis strategy; subsequently, analysis of the same data set was completed using Byonic. Careful assessment of instances where the two methods produced different results revealed that the glycopeptide assignments from Byonic contained more false positives than true positives, even when the data were assessed using a 1% false discovery rate. The work herein provides a roadmap for removing the spurious assignments that Byonic generates, and it provides an assessment of the opportunity cost for relying on automated assignments for glycopeptide data sets from viral glycoproteins. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00216-021-03621-z. Springer Berlin Heidelberg 2021-08-27 2021 /pmc/articles/PMC8390178/ /pubmed/34448030 http://dx.doi.org/10.1007/s00216-021-03621-z Text en © Springer-Verlag GmbH Germany, part of Springer Nature 2021 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Paper in Forefront Go, Eden P. Zhang, Shijian Ding, Haitao Kappes, John C. Sodroski, Joseph Desaire, Heather The opportunity cost of automated glycopeptide analysis: case study profiling the SARS-CoV-2 S glycoprotein |
title | The opportunity cost of automated glycopeptide analysis: case study profiling the SARS-CoV-2 S glycoprotein |
title_full | The opportunity cost of automated glycopeptide analysis: case study profiling the SARS-CoV-2 S glycoprotein |
title_fullStr | The opportunity cost of automated glycopeptide analysis: case study profiling the SARS-CoV-2 S glycoprotein |
title_full_unstemmed | The opportunity cost of automated glycopeptide analysis: case study profiling the SARS-CoV-2 S glycoprotein |
title_short | The opportunity cost of automated glycopeptide analysis: case study profiling the SARS-CoV-2 S glycoprotein |
title_sort | opportunity cost of automated glycopeptide analysis: case study profiling the sars-cov-2 s glycoprotein |
topic | Paper in Forefront |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8390178/ https://www.ncbi.nlm.nih.gov/pubmed/34448030 http://dx.doi.org/10.1007/s00216-021-03621-z |
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