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Proteomic Analysis of Adenovirus 5 by UHPLC-MS/MS: Development of a Robust and Reproducible Sample Preparation Workflow
[Image: see text] Adenoviruses (AdVs) have recently become widely used therapeutic vectors for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccine. AdVs are large, nonenveloped viruses with an icosahedral capsid formed from several proteins that encloses double-stranded DNA. These p...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9583333/ https://www.ncbi.nlm.nih.gov/pubmed/36278084 http://dx.doi.org/10.1021/acsomega.2c05325 |
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author | Zarei, Mostafa Jonveaux, Jérôme Wang, Peng Haller, Friedrich M. Gu, Bingnan Koulov, Atanas V. Jahn, Michael |
author_facet | Zarei, Mostafa Jonveaux, Jérôme Wang, Peng Haller, Friedrich M. Gu, Bingnan Koulov, Atanas V. Jahn, Michael |
author_sort | Zarei, Mostafa |
collection | PubMed |
description | [Image: see text] Adenoviruses (AdVs) have recently become widely used therapeutic vectors for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccine. AdVs are large, nonenveloped viruses with an icosahedral capsid formed from several proteins that encloses double-stranded DNA. These proteins are the main components and key players in initial stages of infection by the virus particles, so their heterogeneity and content must be evaluated to ensure product and process consistency. Peptide mapping can provide detailed information on these proteins, e.g., their amino acid sequences and post-translational modifications (PTMs), which is crucial for the development and optimization of the manufacturing processes. However, sample preparation remains the main bottleneck for successful proteomic analysis of the viral proteins (VPs) of AdVs due to their low concentrations and vast stoichiometric ranges. To address this problem, we have developed a fast and efficient protocol for preparing samples for proteomic analysis of VPs of AdV5 that requires no cleaning step prior to liquid chromatography–tandem mass spectrometry (LC-MS/MS). The approach enabled identification of 92% of amino acids in AdV5 VPs on average and quantification of 53 PTMs in a single LC-MS/MS experiment using trypsin protease. The data obtained demonstrate the method’s potential utility for supporting the development of novel AdV-based gene therapy products (GTPs). |
format | Online Article Text |
id | pubmed-9583333 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-95833332022-10-21 Proteomic Analysis of Adenovirus 5 by UHPLC-MS/MS: Development of a Robust and Reproducible Sample Preparation Workflow Zarei, Mostafa Jonveaux, Jérôme Wang, Peng Haller, Friedrich M. Gu, Bingnan Koulov, Atanas V. Jahn, Michael ACS Omega [Image: see text] Adenoviruses (AdVs) have recently become widely used therapeutic vectors for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccine. AdVs are large, nonenveloped viruses with an icosahedral capsid formed from several proteins that encloses double-stranded DNA. These proteins are the main components and key players in initial stages of infection by the virus particles, so their heterogeneity and content must be evaluated to ensure product and process consistency. Peptide mapping can provide detailed information on these proteins, e.g., their amino acid sequences and post-translational modifications (PTMs), which is crucial for the development and optimization of the manufacturing processes. However, sample preparation remains the main bottleneck for successful proteomic analysis of the viral proteins (VPs) of AdVs due to their low concentrations and vast stoichiometric ranges. To address this problem, we have developed a fast and efficient protocol for preparing samples for proteomic analysis of VPs of AdV5 that requires no cleaning step prior to liquid chromatography–tandem mass spectrometry (LC-MS/MS). The approach enabled identification of 92% of amino acids in AdV5 VPs on average and quantification of 53 PTMs in a single LC-MS/MS experiment using trypsin protease. The data obtained demonstrate the method’s potential utility for supporting the development of novel AdV-based gene therapy products (GTPs). American Chemical Society 2022-10-05 /pmc/articles/PMC9583333/ /pubmed/36278084 http://dx.doi.org/10.1021/acsomega.2c05325 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Zarei, Mostafa Jonveaux, Jérôme Wang, Peng Haller, Friedrich M. Gu, Bingnan Koulov, Atanas V. Jahn, Michael Proteomic Analysis of Adenovirus 5 by UHPLC-MS/MS: Development of a Robust and Reproducible Sample Preparation Workflow |
title | Proteomic Analysis
of Adenovirus 5 by UHPLC-MS/MS:
Development of a Robust and Reproducible Sample Preparation Workflow |
title_full | Proteomic Analysis
of Adenovirus 5 by UHPLC-MS/MS:
Development of a Robust and Reproducible Sample Preparation Workflow |
title_fullStr | Proteomic Analysis
of Adenovirus 5 by UHPLC-MS/MS:
Development of a Robust and Reproducible Sample Preparation Workflow |
title_full_unstemmed | Proteomic Analysis
of Adenovirus 5 by UHPLC-MS/MS:
Development of a Robust and Reproducible Sample Preparation Workflow |
title_short | Proteomic Analysis
of Adenovirus 5 by UHPLC-MS/MS:
Development of a Robust and Reproducible Sample Preparation Workflow |
title_sort | proteomic analysis
of adenovirus 5 by uhplc-ms/ms:
development of a robust and reproducible sample preparation workflow |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9583333/ https://www.ncbi.nlm.nih.gov/pubmed/36278084 http://dx.doi.org/10.1021/acsomega.2c05325 |
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