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首页> 外文期刊>Scientific reports. >The In Vitro Biotransformation of the Fusion Protein Tetranectin-Apolipoprotein A1
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The In Vitro Biotransformation of the Fusion Protein Tetranectin-Apolipoprotein A1

机译:融合蛋白Tetranectin-载脂蛋白A1的体外生物转化

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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.
机译:随着越来越多的蛋白质生物治疗药物进入药物发现管道,人们越来越关注生物制剂的机械药物代谢研究工具,以便确定最有希望的候选药物并对其进行优先级排序。了解甚至预测生物制剂的体内清除率并支持翻译药代动力学建模活动是必不可少的,但是缺少有效且经过验证的体外细胞工具。尽管在生物制剂的处置中必须解决不同的机制,但是其范围与当今广泛建立的用于小分子处置的早期表征的工具无法相比。在这里,我们描述了通过细胞系统对融合蛋白四连蛋白载脂蛋白A1的生物转化研究。先前已经描述了四连蛋白载脂蛋白A1的体内生物转化,并且还可以通过基于胰凝乳蛋白酶消化的靶向且高度灵敏的检测方法在体外检测到相同的主要生物转化产物。另外,负责该生物转化产物形成的蛋白酶可以被阐明为DPP4。据我们所知,这是治疗性蛋白质细胞进行体外生物转化研究的首批报告之一。

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