Abstract

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.

Highlights

  • Protein biotherapeutics are a class of pharmaceutical drugs with increasing importance for the treatment of various diseases

  • We describe the investigation and application of in vitro cellular systems for the biotransformation of the therapeutic fusion protein tetranectin apolipoprotein A1 (TN-ApoA1)

  • Hoffmann-La Roche Ltd. (Basel, Switzerland). 2,2,2-Trifluoroacetic acid (TFA), Gibco fetal calf serum (FCS), Gibco DPBS buffer, Pierce magnetic beads coated with streptavidin (10 mg/mL) and Chymotrypsin smart digest kit were purchased from Thermo Fisher Scientific (Rheinach, Switzerland), as well as the custom-synthesized reference peptides APIVNAKKDVVNTKMF and IVNAKKDVVNTKMF

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Summary

Introduction

Protein biotherapeutics are a class of pharmaceutical drugs with increasing importance for the treatment of various diseases. Incubation of TN-ApoA1 with RPTEC/TERT1 cells and primary HUVEC cells. Formation of the major catabolite [3-285] of TN-ApoA1 by with DPP4, in RPTEC/TERT1 and HUVEC cells was investigated.

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