Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Schadt, Simone, Husser, Christophe, Staack, Roland F., Ekiciler, Aynur, Qiu, Na Hong, Fowler, Stephen, Funk, Christoph, Kratochwil, Nicole A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
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
_version_ 1783402476489146368
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
work_keys_str_mv AT schadtsimone theinvitrobiotransformationofthefusionproteintetranectinapolipoproteina1
AT husserchristophe theinvitrobiotransformationofthefusionproteintetranectinapolipoproteina1
AT staackrolandf theinvitrobiotransformationofthefusionproteintetranectinapolipoproteina1
AT ekicileraynur theinvitrobiotransformationofthefusionproteintetranectinapolipoproteina1
AT qiunahong theinvitrobiotransformationofthefusionproteintetranectinapolipoproteina1
AT fowlerstephen theinvitrobiotransformationofthefusionproteintetranectinapolipoproteina1
AT funkchristoph theinvitrobiotransformationofthefusionproteintetranectinapolipoproteina1
AT kratochwilnicolea theinvitrobiotransformationofthefusionproteintetranectinapolipoproteina1
AT schadtsimone invitrobiotransformationofthefusionproteintetranectinapolipoproteina1
AT husserchristophe invitrobiotransformationofthefusionproteintetranectinapolipoproteina1
AT staackrolandf invitrobiotransformationofthefusionproteintetranectinapolipoproteina1
AT ekicileraynur invitrobiotransformationofthefusionproteintetranectinapolipoproteina1
AT qiunahong invitrobiotransformationofthefusionproteintetranectinapolipoproteina1
AT fowlerstephen invitrobiotransformationofthefusionproteintetranectinapolipoproteina1
AT funkchristoph invitrobiotransformationofthefusionproteintetranectinapolipoproteina1
AT kratochwilnicolea invitrobiotransformationofthefusionproteintetranectinapolipoproteina1