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The In Vitro Biotransformation of the Fusion Protein Tetranectin-Apolipoprotein A1
As more and more protein biotherapeutics enter the drug discovery pipelines, there is an increasing interest in tools for mechanistic drug metabolism investigations of biologics in order to identify and prioritize the most promising candidates. Understanding or even predicting the in vivo clearance...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6411889/ https://www.ncbi.nlm.nih.gov/pubmed/30858459 http://dx.doi.org/10.1038/s41598-019-40542-5 |
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author | Schadt, Simone Husser, Christophe Staack, Roland F. Ekiciler, Aynur Qiu, Na Hong Fowler, Stephen Funk, Christoph Kratochwil, Nicole A. |
author_facet | Schadt, Simone Husser, Christophe Staack, Roland F. Ekiciler, Aynur Qiu, Na Hong Fowler, Stephen Funk, Christoph Kratochwil, Nicole A. |
author_sort | Schadt, Simone |
collection | PubMed |
description | As more and more protein biotherapeutics enter the drug discovery pipelines, there is an increasing interest in tools for mechanistic drug metabolism investigations of biologics in order to identify and prioritize the most promising candidates. Understanding or even predicting the in vivo clearance of biologics and to support translational pharmacokinetic modeling activities is essential, however there is a lack of effective and validated in vitro cellular tools. Although different mechanisms have to be adressed in the context of biologics disposition, the scope is not comparable to the nowadays widely established tools for early characterization of small molecule disposition. Here, we describe a biotransformation study of the fusion protein tetranectin apolipoprotein A1 by cellular systems. The in vivo biotransformation of tetranectin apolipoprotein A1 has been described previously, and the same major biotransformation product could also be detected in vitro, by a targeted and highly sensitive detection method based on chymotrypsin digest. In addition, the protease responsible for the formation of this biotransformation product could be elucidated to be DPP4. To our knowledge, this is one of the first reports of an in vitro biotransformation study by cells of a therapeutic protein. |
format | Online Article Text |
id | pubmed-6411889 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-64118892019-03-13 The In Vitro Biotransformation of the Fusion Protein Tetranectin-Apolipoprotein A1 Schadt, Simone Husser, Christophe Staack, Roland F. Ekiciler, Aynur Qiu, Na Hong Fowler, Stephen Funk, Christoph Kratochwil, Nicole A. Sci Rep Article As more and more protein biotherapeutics enter the drug discovery pipelines, there is an increasing interest in tools for mechanistic drug metabolism investigations of biologics in order to identify and prioritize the most promising candidates. Understanding or even predicting the in vivo clearance of biologics and to support translational pharmacokinetic modeling activities is essential, however there is a lack of effective and validated in vitro cellular tools. Although different mechanisms have to be adressed in the context of biologics disposition, the scope is not comparable to the nowadays widely established tools for early characterization of small molecule disposition. Here, we describe a biotransformation study of the fusion protein tetranectin apolipoprotein A1 by cellular systems. The in vivo biotransformation of tetranectin apolipoprotein A1 has been described previously, and the same major biotransformation product could also be detected in vitro, by a targeted and highly sensitive detection method based on chymotrypsin digest. In addition, the protease responsible for the formation of this biotransformation product could be elucidated to be DPP4. To our knowledge, this is one of the first reports of an in vitro biotransformation study by cells of a therapeutic protein. Nature Publishing Group UK 2019-03-11 /pmc/articles/PMC6411889/ /pubmed/30858459 http://dx.doi.org/10.1038/s41598-019-40542-5 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Schadt, Simone Husser, Christophe Staack, Roland F. Ekiciler, Aynur Qiu, Na Hong Fowler, Stephen Funk, Christoph Kratochwil, Nicole A. The In Vitro Biotransformation of the Fusion Protein Tetranectin-Apolipoprotein A1 |
title | The In Vitro Biotransformation of the Fusion Protein Tetranectin-Apolipoprotein A1 |
title_full | The In Vitro Biotransformation of the Fusion Protein Tetranectin-Apolipoprotein A1 |
title_fullStr | The In Vitro Biotransformation of the Fusion Protein Tetranectin-Apolipoprotein A1 |
title_full_unstemmed | The In Vitro Biotransformation of the Fusion Protein Tetranectin-Apolipoprotein A1 |
title_short | The In Vitro Biotransformation of the Fusion Protein Tetranectin-Apolipoprotein A1 |
title_sort | in vitro biotransformation of the fusion protein tetranectin-apolipoprotein a1 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6411889/ https://www.ncbi.nlm.nih.gov/pubmed/30858459 http://dx.doi.org/10.1038/s41598-019-40542-5 |
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