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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...

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Autores principales: Lerch, Thomas F., Sharpe, Penelope, Mayclin, Stephen J., Edwards, Thomas E., Polleck, Sharon, Rouse, Jason C., Zou, Qin, Conlon, Hugh D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2019
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.
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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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