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At-line high throughput site-specific glycan profiling using targeted mass spectrometry
Protein post-translational modification (PTM) plays an important role in many biological processes; of which glycosylation is arguably one of the most complex and diverse modifications and is crucial for the safety and efficacy of biotherapeutic proteins. Mass spectrometric characterization of prote...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7016254/ https://www.ncbi.nlm.nih.gov/pubmed/32071892 http://dx.doi.org/10.1016/j.btre.2020.e00424 |
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author | Chi, Bertie Veyssier, Christel Kasali, Toyin Uddin, Faisal Sellick, Christopher A. |
author_facet | Chi, Bertie Veyssier, Christel Kasali, Toyin Uddin, Faisal Sellick, Christopher A. |
author_sort | Chi, Bertie |
collection | PubMed |
description | Protein post-translational modification (PTM) plays an important role in many biological processes; of which glycosylation is arguably one of the most complex and diverse modifications and is crucial for the safety and efficacy of biotherapeutic proteins. Mass spectrometric characterization of protein glycosylation is well established with clear advantages and disadvantages; on one hand it is precise and information-rich, as well as being relative inexpensive in terms of the reagents and consumables despite the instrumentation cost and, depending on the method, can give site specific information; on the other hand it generally suffers from low throughput, restriction to largely purified samples and is less quantitative, especially for sialylated glycan species. Here, we describe a high throughput, site-specific, targeted mass spectrometric peptide mapping approach to quickly screen/rank candidate production cell lines and culture conditions that give favourable glycosylation profiles directly from conditioned culture media for an Fc-fusion protein. The methodology is fully compatible with automation and combines the speed of ‘top-down’ mass spectrometry with the site-specific information of ‘bottom-up’ mass spectrometry. In addition, this strategy can be used for multi-attribute product quality screening/monitoring as an integral part of cell line selection and process development. |
format | Online Article Text |
id | pubmed-7016254 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-70162542020-02-18 At-line high throughput site-specific glycan profiling using targeted mass spectrometry Chi, Bertie Veyssier, Christel Kasali, Toyin Uddin, Faisal Sellick, Christopher A. Biotechnol Rep (Amst) Research Article Protein post-translational modification (PTM) plays an important role in many biological processes; of which glycosylation is arguably one of the most complex and diverse modifications and is crucial for the safety and efficacy of biotherapeutic proteins. Mass spectrometric characterization of protein glycosylation is well established with clear advantages and disadvantages; on one hand it is precise and information-rich, as well as being relative inexpensive in terms of the reagents and consumables despite the instrumentation cost and, depending on the method, can give site specific information; on the other hand it generally suffers from low throughput, restriction to largely purified samples and is less quantitative, especially for sialylated glycan species. Here, we describe a high throughput, site-specific, targeted mass spectrometric peptide mapping approach to quickly screen/rank candidate production cell lines and culture conditions that give favourable glycosylation profiles directly from conditioned culture media for an Fc-fusion protein. The methodology is fully compatible with automation and combines the speed of ‘top-down’ mass spectrometry with the site-specific information of ‘bottom-up’ mass spectrometry. In addition, this strategy can be used for multi-attribute product quality screening/monitoring as an integral part of cell line selection and process development. Elsevier 2020-01-22 /pmc/articles/PMC7016254/ /pubmed/32071892 http://dx.doi.org/10.1016/j.btre.2020.e00424 Text en © 2020 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Research Article Chi, Bertie Veyssier, Christel Kasali, Toyin Uddin, Faisal Sellick, Christopher A. At-line high throughput site-specific glycan profiling using targeted mass spectrometry |
title | At-line high throughput site-specific glycan profiling using targeted mass spectrometry |
title_full | At-line high throughput site-specific glycan profiling using targeted mass spectrometry |
title_fullStr | At-line high throughput site-specific glycan profiling using targeted mass spectrometry |
title_full_unstemmed | At-line high throughput site-specific glycan profiling using targeted mass spectrometry |
title_short | At-line high throughput site-specific glycan profiling using targeted mass spectrometry |
title_sort | at-line high throughput site-specific glycan profiling using targeted mass spectrometry |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7016254/ https://www.ncbi.nlm.nih.gov/pubmed/32071892 http://dx.doi.org/10.1016/j.btre.2020.e00424 |
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