Rustandi Richard R, Hamm Melissa, Lancaster Catherine, Loughney John W
Merck Research Laboratories, Vaccine Analytical Development, 770 Sumneytown Pike, WP42A-30, P.O. Box 4, West Point, PA, 19486, USA.
Methods Mol Biol. 2016;1466:197-217. doi: 10.1007/978-1-4939-4014-1_16.
Capillary Electrophoresis (CE) is a versatile and indispensable analytical tool that can be applied to characterize proteins. In recent years, labor-intensive SDS-PAGE and IEF slab gels have been replaced with CE-SDS (CGE) and CE-IEF methods, respectively, in the biopharmaceutical industry. These two CE-based methods are now an industry standard and are an expectation of the regulatory agencies for biologics characterization. Another important and traditional slab gel technique is the western blot, which detects proteins using immuno-specific reagents after SDS-PAGE separation. This technique is widely used across industrial and academic laboratories, but it is very laborious, manual, time-consuming, and only semi-quantitative. Here, we describe the applications of a relatively new CE-based western blot technology which is automated, fast, and quantitative. We have used this technology for both charge- and size-based CE westerns to analyze biotherapeutic and vaccine products. The size-based capillary western can be used for fast antibody screening, clone selection, product titer, identity, and degradation while the charge-based capillary western can be used to study product charge heterogeneity. Examples using this technology for monoclonal antibody (mAb), Enbrel, CRM197, and Clostridium difficile (C. difficile) vaccine proteins are presented here to demonstrate the utility of the capillary western techniques. Details of sample preparation and experimental conditions for each capillary western mode are described in this chapter.
毛细管电泳(CE)是一种通用且不可或缺的分析工具,可用于表征蛋白质。近年来,生物制药行业中劳动强度大的SDS-PAGE和IEF平板凝胶已分别被CE-SDS(CGE)和CE-IEF方法所取代。这两种基于CE的方法现已成为行业标准,也是监管机构对生物制品表征的期望。另一种重要且传统的平板凝胶技术是蛋白质印迹法,它在SDS-PAGE分离后使用免疫特异性试剂检测蛋白质。该技术在工业和学术实验室中广泛使用,但非常费力、手工操作、耗时且只是半定量的。在此,我们描述一种相对较新的基于CE的蛋白质印迹技术的应用,该技术自动化、快速且定量。我们已将此技术用于基于电荷和大小的CE蛋白质印迹,以分析生物治疗药物和疫苗产品。基于大小的毛细管蛋白质印迹可用于快速抗体筛选、克隆选择、产品效价、鉴定和降解分析,而基于电荷的毛细管蛋白质印迹可用于研究产品电荷异质性。本文展示了使用该技术分析单克隆抗体(mAb)、恩利、CRM197和艰难梭菌疫苗蛋白的实例,以证明毛细管蛋白质印迹技术的实用性。本章描述了每种毛细管蛋白质印迹模式的样品制备细节和实验条件。