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Crystal Structures of PF-06438179/GP1111, an Infliximab Biosimilar
BACKGROUND: Higher-order structure (HOS) assessment is an important component of biosimilarity evaluations. While established spectroscopic methods are routinely used to characterize structure and evaluate similarity, the addition of X-ray crystallographic analysis to these biophysical methods enabl...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6985046/ https://www.ncbi.nlm.nih.gov/pubmed/31650490 http://dx.doi.org/10.1007/s40259-019-00390-1 |
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author | Lerch, Thomas F. Sharpe, Penelope Mayclin, Stephen J. Edwards, Thomas E. Polleck, Sharon Rouse, Jason C. Zou, Qin Conlon, Hugh D. |
author_facet | Lerch, Thomas F. Sharpe, Penelope Mayclin, Stephen J. Edwards, Thomas E. Polleck, Sharon Rouse, Jason C. Zou, Qin Conlon, Hugh D. |
author_sort | Lerch, Thomas F. |
collection | PubMed |
description | BACKGROUND: Higher-order structure (HOS) assessment is an important component of biosimilarity evaluations. While established spectroscopic methods are routinely used to characterize structure and evaluate similarity, the addition of X-ray crystallographic analysis to these biophysical methods enables orthogonal elucidation of HOS at higher resolution. METHODS: Crystal structures of the infliximab biosimilar PF-06438179/GP1111 and the reference product Remicade(®), sourced from US and European Union markets, were determined and compared to evaluate HOS similarity. Analytical ultracentrifugation studies were conducted to understand reversible self-association. RESULTS: In contrast to more routine spectroscopic methods, the crystal structures enable three-dimensional assessment of complementarity-determining regions and other local regions at near-atomic resolution. The biosimilar structures are highly similar to those of the reference product, as demonstrated visually and though all-atom root-mean-squared deviation measurements. CONCLUSION: The structures provide new insights into the physicochemical properties of the proposed biosimilar and the reference product, further strengthening the ‘totality of evidence’ in the evaluation of similarity. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s40259-019-00390-1) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6985046 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-69850462020-02-07 Crystal Structures of PF-06438179/GP1111, an Infliximab Biosimilar Lerch, Thomas F. Sharpe, Penelope Mayclin, Stephen J. Edwards, Thomas E. Polleck, Sharon Rouse, Jason C. Zou, Qin Conlon, Hugh D. BioDrugs Original Research Article BACKGROUND: Higher-order structure (HOS) assessment is an important component of biosimilarity evaluations. While established spectroscopic methods are routinely used to characterize structure and evaluate similarity, the addition of X-ray crystallographic analysis to these biophysical methods enables orthogonal elucidation of HOS at higher resolution. METHODS: Crystal structures of the infliximab biosimilar PF-06438179/GP1111 and the reference product Remicade(®), sourced from US and European Union markets, were determined and compared to evaluate HOS similarity. Analytical ultracentrifugation studies were conducted to understand reversible self-association. RESULTS: In contrast to more routine spectroscopic methods, the crystal structures enable three-dimensional assessment of complementarity-determining regions and other local regions at near-atomic resolution. The biosimilar structures are highly similar to those of the reference product, as demonstrated visually and though all-atom root-mean-squared deviation measurements. CONCLUSION: The structures provide new insights into the physicochemical properties of the proposed biosimilar and the reference product, further strengthening the ‘totality of evidence’ in the evaluation of similarity. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s40259-019-00390-1) contains supplementary material, which is available to authorized users. Springer International Publishing 2019-10-24 2020 /pmc/articles/PMC6985046/ /pubmed/31650490 http://dx.doi.org/10.1007/s40259-019-00390-1 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/), which permits any noncommercial use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Research Article Lerch, Thomas F. Sharpe, Penelope Mayclin, Stephen J. Edwards, Thomas E. Polleck, Sharon Rouse, Jason C. Zou, Qin Conlon, Hugh D. Crystal Structures of PF-06438179/GP1111, an Infliximab Biosimilar |
title | Crystal Structures of PF-06438179/GP1111, an Infliximab Biosimilar |
title_full | Crystal Structures of PF-06438179/GP1111, an Infliximab Biosimilar |
title_fullStr | Crystal Structures of PF-06438179/GP1111, an Infliximab Biosimilar |
title_full_unstemmed | Crystal Structures of PF-06438179/GP1111, an Infliximab Biosimilar |
title_short | Crystal Structures of PF-06438179/GP1111, an Infliximab Biosimilar |
title_sort | crystal structures of pf-06438179/gp1111, an infliximab biosimilar |
topic | Original Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6985046/ https://www.ncbi.nlm.nih.gov/pubmed/31650490 http://dx.doi.org/10.1007/s40259-019-00390-1 |
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