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Determination of the degree of PEGylation of protein bioconjugates using data from proton nuclear magnetic resonance spectroscopy
The average number of methoxy poly(ethylene glycol) (mPEG) chains grafted to a protein – also known as the degree of PEGylation – is a fundamental parameter for characterizing a bioconjugate. The degree of PEGylation is typically determined by chromatographic or electrophoretic methods, which are su...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6565728/ https://www.ncbi.nlm.nih.gov/pubmed/31223640 http://dx.doi.org/10.1016/j.dib.2019.104037 |
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author | Zaghmi, Ahlem Greschner, Andrea A. Mendez-Villuendas, Eduardo Liu, Jun Yang de Haan, Hendrick W. Gauthier, Marc A. |
author_facet | Zaghmi, Ahlem Greschner, Andrea A. Mendez-Villuendas, Eduardo Liu, Jun Yang de Haan, Hendrick W. Gauthier, Marc A. |
author_sort | Zaghmi, Ahlem |
collection | PubMed |
description | The average number of methoxy poly(ethylene glycol) (mPEG) chains grafted to a protein – also known as the degree of PEGylation – is a fundamental parameter for characterizing a bioconjugate. The degree of PEGylation is typically determined by chromatographic or electrophoretic methods, which are subject to certain biases. This contribution describes an analytical approach alongside technical precautions for quantitatively determining the degree of PEGylation of protein bioconjugates by (1)H NMR spectroscopy. An accompanying dataset, corresponding to the raw (1)H NMR spectra of thirteen bioconjugates with different degrees of PEGylation and different mPEG molecular weights, is provided for the reader to become familiar with the analysis. The exemplary bioconjugate system used in this Data article is the enzyme glutamate dehydrogenase (GDH) modified with multiple copies of mPEG (0.5–20 kDa). These bioconjugates correspond to those discussed in-depth in the article “Mechanisms of activity loss for a multi-PEGylated protein by experiment and simulation” by Zaghmi et al., 2019 The described approach to calculate degree of PEGylation is quantitative, applicable to other proteins, and can be adapted to other types of polymers. |
format | Online Article Text |
id | pubmed-6565728 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-65657282019-06-20 Determination of the degree of PEGylation of protein bioconjugates using data from proton nuclear magnetic resonance spectroscopy Zaghmi, Ahlem Greschner, Andrea A. Mendez-Villuendas, Eduardo Liu, Jun Yang de Haan, Hendrick W. Gauthier, Marc A. Data Brief Biochemistry, Genetics and Molecular Biology The average number of methoxy poly(ethylene glycol) (mPEG) chains grafted to a protein – also known as the degree of PEGylation – is a fundamental parameter for characterizing a bioconjugate. The degree of PEGylation is typically determined by chromatographic or electrophoretic methods, which are subject to certain biases. This contribution describes an analytical approach alongside technical precautions for quantitatively determining the degree of PEGylation of protein bioconjugates by (1)H NMR spectroscopy. An accompanying dataset, corresponding to the raw (1)H NMR spectra of thirteen bioconjugates with different degrees of PEGylation and different mPEG molecular weights, is provided for the reader to become familiar with the analysis. The exemplary bioconjugate system used in this Data article is the enzyme glutamate dehydrogenase (GDH) modified with multiple copies of mPEG (0.5–20 kDa). These bioconjugates correspond to those discussed in-depth in the article “Mechanisms of activity loss for a multi-PEGylated protein by experiment and simulation” by Zaghmi et al., 2019 The described approach to calculate degree of PEGylation is quantitative, applicable to other proteins, and can be adapted to other types of polymers. Elsevier 2019-05-23 /pmc/articles/PMC6565728/ /pubmed/31223640 http://dx.doi.org/10.1016/j.dib.2019.104037 Text en © 2019 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Biochemistry, Genetics and Molecular Biology Zaghmi, Ahlem Greschner, Andrea A. Mendez-Villuendas, Eduardo Liu, Jun Yang de Haan, Hendrick W. Gauthier, Marc A. Determination of the degree of PEGylation of protein bioconjugates using data from proton nuclear magnetic resonance spectroscopy |
title | Determination of the degree of PEGylation of protein bioconjugates using data from proton nuclear magnetic resonance spectroscopy |
title_full | Determination of the degree of PEGylation of protein bioconjugates using data from proton nuclear magnetic resonance spectroscopy |
title_fullStr | Determination of the degree of PEGylation of protein bioconjugates using data from proton nuclear magnetic resonance spectroscopy |
title_full_unstemmed | Determination of the degree of PEGylation of protein bioconjugates using data from proton nuclear magnetic resonance spectroscopy |
title_short | Determination of the degree of PEGylation of protein bioconjugates using data from proton nuclear magnetic resonance spectroscopy |
title_sort | determination of the degree of pegylation of protein bioconjugates using data from proton nuclear magnetic resonance spectroscopy |
topic | Biochemistry, Genetics and Molecular Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6565728/ https://www.ncbi.nlm.nih.gov/pubmed/31223640 http://dx.doi.org/10.1016/j.dib.2019.104037 |
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