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用于双特异性和多特异性抗体高通量筛选和表征的全长蛋白质质谱分析的端到端自动化

End-To-End Automated Intact Protein Mass Spectrometry for High-Throughput Screening and Characterization of Bispecific and Multispecific Antibodies.

机构信息

Department of Discovery Biotherapeutics, Bristol Myers Squibb, San Diego, California 92121, United States.

出版信息

Anal Chem. 2024 Nov 12;96(45):18287-18300. doi: 10.1021/acs.analchem.4c04833. Epub 2024 Oct 31.

Abstract

Bispecific antibodies (bsAbs) and multispecific antibodies (msAbs) represent a promising frontier in therapeutic antibody development, offering unique capabilities not achievable with traditional monoclonal antibodies. Despite their potential, significant challenges remain due to their increased molecular complexity. One prominent challenge is the correct assembly of light and heavy chains, as improper pairing leads to mispaired or incompletely assembled species that lack therapeutic efficacy and possess undesired properties, impairing the developability, manufacturability, and safety. There is a critical need for rapid, sensitive analytical tools to monitor and control these undesired species and ensure the quality assessment of bsAbs and msAbs. To address this need, we present a novel high-throughput, format-agnostic intact mass workflow that significantly enhances the efficiency of detecting and quantifying biotherapeutic products and related impurities. This workflow integrates automated sample preparation, novel high-resolution rapid mass detection powered by SampleStream-MS, and an advanced data analysis pipeline. It offers increased throughput and data quality while substantially reducing analysis turnover time and labor. This was demonstrated in a pilot program where ∼800 multispecific antibodies were processed in 10 working days. The article details the evaluation and validation of our method, demonstrating its repeatability and intermediate precision in terms of measurement accuracy and relative quantification of various product-related species. We underscore the transformative potential of this end-to-end high-throughput workflow in expediting bispecific and multispecific antibody discovery, optimizing production processes, and ensuring high-quality development and manufacturing for therapeutic antibodies.

摘要

双特异性抗体 (bsAbs) 和多特异性抗体 (msAbs) 代表了治疗性抗体开发的一个有前途的前沿领域,提供了传统单克隆抗体无法实现的独特功能。尽管它们具有潜力,但由于其分子复杂性增加,仍然存在重大挑战。一个突出的挑战是正确组装轻链和重链,因为不正确的配对会导致错配或不完全组装的物种,缺乏治疗效果,并具有不理想的性质,从而影响可开发性、可制造性和安全性。迫切需要快速、灵敏的分析工具来监测和控制这些不理想的物种,并确保 bsAbs 和 msAbs 的质量评估。为了满足这一需求,我们提出了一种新颖的高通量、无格式整体质量工作流程,可显著提高检测和定量生物治疗产品和相关杂质的效率。该工作流程集成了自动化样品制备、由 SampleStream-MS 提供的新型高分辨率快速质量检测以及先进的数据分析管道。它提高了通量和数据质量,同时大大缩短了分析周转时间和劳动力。这在一个试点项目中得到了证明,该项目在 10 个工作日内处理了约 800 种多特异性抗体。本文详细介绍了我们方法的评估和验证,证明了其在测量准确性和各种产品相关物种的相对定量方面的重复性和中间精度。我们强调了这种端到端高通量工作流程在加速双特异性和多特异性抗体发现、优化生产工艺以及确保治疗性抗体的高质量开发和制造方面的变革潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f68/11562946/c2cfcf9e4fc8/ac4c04833_0001.jpg

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