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融合蛋白四连接蛋白-载脂蛋白 A1 的体外生物转化。

The In Vitro Biotransformation of the Fusion Protein Tetranectin-Apolipoprotein A1.

机构信息

Roche Pharma Research and Early Development, Roche Innovation Center Basel, F. Hoffmann-La Roche Ltd, Grenzacherstr. 124, CH-4070, Basel, Switzerland.

Roche Pharma Research and Early Development, Roche Innovation Center Munich, Roche Diagnostics GmbH, Nonnenwald 2, 82377, Penzberg, Germany.

出版信息

Sci Rep. 2019 Mar 11;9(1):4074. doi: 10.1038/s41598-019-40542-5.

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.

摘要

随着越来越多的蛋白质生物治疗药物进入药物发现管道,人们对用于研究生物药物的机制药物代谢的工具越来越感兴趣,以确定和优先考虑最有前途的候选药物。了解甚至预测生物药物的体内清除率,并支持转化药代动力学建模活动是至关重要的,但目前缺乏有效的和经过验证的体外细胞工具。尽管在生物药物处置的背景下必须考虑不同的机制,但范围与目前广泛用于小分子处置早期特征描述的工具不可比。在这里,我们描述了通过细胞系统对融合蛋白四连接蛋白载脂蛋白 A1 的生物转化研究。四连接蛋白载脂蛋白 A1 的体内生物转化以前已有描述,并且通过基于糜蛋白酶消化的靶向和高灵敏度检测方法也可以在体外检测到相同的主要生物转化产物。此外,还可以阐明负责形成这种生物转化产物的蛋白酶是 DPP4。据我们所知,这是细胞对治疗性蛋白质进行体外生物转化研究的首批报告之一。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ca5/6411889/25483c563545/41598_2019_40542_Fig1_HTML.jpg

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