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血清中免疫分离的人治疗性抗体的完整质谱分析

Intact Mass Spectrometry Analysis of Immuno-Isolated Human Therapeutic Antibodies from Serum.

作者信息

Delaney Christie E, Kelly John F, Ding Wen, Haqqani Arsalan S

机构信息

Human Health Therapeutics Research Centre, National Research Council of Canada, Ottawa, ON, Canada.

出版信息

Methods Mol Biol. 2019;2024:153-166. doi: 10.1007/978-1-4939-9597-4_9.

Abstract

Antibody-based therapeutics have emerged as novel class of biopharmaceuticals over the last couple of decades with the advancements made in production and downstream processing technologies. The structural diversity of therapeutic antibodies has also evolved with the development of bispecific (and multispecific) antibodies and antibody-drug conjugates. With increased structural complexities and multi-modularity, there is a need to demonstrate that the entire structure is stable in vivo and arriving at its target site in an intact form. Proving that antibodies reach their target site unscathed is a challenging but essential step for showing effective delivery as well as showing whether failure in efficacy (if any) was related to its in vivo instability. This chapter describes a method for highly specific immuno-isolation followed by intact mass spectrometry of human Fc-containing antibody from serum of rats dosed with the antibody. The method provides an opportunity for evaluating antibody stability in the physiological environment by providing accurate validation of its molecular mass in vivo, as well as the potential to identify breakdown products.

摘要

在过去几十年里,随着生产和下游加工技术的进步,基于抗体的治疗药物已成为一类新型生物制药。随着双特异性(及多特异性)抗体和抗体药物偶联物的发展,治疗性抗体的结构多样性也在不断演变。随着结构复杂性和多模块性的增加,有必要证明整个结构在体内是稳定的,并以完整的形式到达其靶位点。证明抗体毫发无损地到达其靶位点是一个具有挑战性但又至关重要的步骤,这对于展示有效递送以及表明疗效失败(如果有的话)是否与其体内不稳定性有关。本章描述了一种从给予抗体的大鼠血清中高度特异性免疫分离含人Fc抗体,然后进行完整质谱分析的方法。该方法通过在体内准确验证其分子量,为评估抗体在生理环境中的稳定性提供了机会,同时也有识别降解产物的潜力。

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