Chi Bertie, Veyssier Christel, Kasali Toyin, Uddin Faisal, Sellick Christopher A
MedImmune, Milstein Building, Granta Park, Cambridge, CB21 6GH, UK.
Biotechnol Rep (Amst). 2020 Jan 22;25:e00424. doi: 10.1016/j.btre.2020.e00424. eCollection 2020 Mar.
Protein post-translational modification (PTM) plays an important role in many biological processes; of which glycosylation is arguably one of the most complex and diverse modifications and is crucial for the safety and efficacy of biotherapeutic proteins. Mass spectrometric characterization of protein glycosylation is well established with clear advantages and disadvantages; on one hand it is precise and information-rich, as well as being relative inexpensive in terms of the reagents and consumables despite the instrumentation cost and, depending on the method, can give site specific information; on the other hand it generally suffers from low throughput, restriction to largely purified samples and is less quantitative, especially for sialylated glycan species. Here, we describe a high throughput, site-specific, targeted mass spectrometric peptide mapping approach to quickly screen/rank candidate production cell lines and culture conditions that give favourable glycosylation profiles directly from conditioned culture media for an Fc-fusion protein. The methodology is fully compatible with automation and combines the speed of 'top-down' mass spectrometry with the site-specific information of 'bottom-up' mass spectrometry. In addition, this strategy can be used for multi-attribute product quality screening/monitoring as an integral part of cell line selection and process development.
蛋白质翻译后修饰(PTM)在许多生物学过程中发挥着重要作用;其中糖基化可以说是最复杂、最多样化的修饰之一,对生物治疗蛋白的安全性和有效性至关重要。蛋白质糖基化的质谱表征已得到充分确立,有明显的优缺点;一方面,它精确且信息丰富,尽管仪器成本较高,但就试剂和耗材而言相对便宜,并且根据方法不同,能够提供位点特异性信息;另一方面,它通常通量较低,主要限于纯化的样品,定量性较差,尤其是对于唾液酸化聚糖种类。在此,我们描述了一种高通量、位点特异性、靶向质谱肽图谱分析方法,用于快速筛选/排名候选生产细胞系和培养条件,这些条件可直接从Fc融合蛋白的条件培养基中获得有利的糖基化谱。该方法完全与自动化兼容,将“自上而下”质谱的速度与“自下而上”质谱的位点特异性信息相结合。此外,该策略可作为细胞系选择和工艺开发的一个组成部分,用于多属性产品质量筛选/监测。