Zhang Chao-Xuan, Meagher Michael M
Department of Therapeutics Production and Quality, St. Jude Children's Research Hospital, Memphis, TN, USA.
Methods Mol Biol. 2019;1972:263-270. doi: 10.1007/978-1-4939-9213-3_19.
Sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) has been the method of choice in the past decades for size-based protein analysis. However, in general it requires the protein concentration in mg/mL level and thus is not practical for trace level protein analysis, not to mention the lengthy labor-intensive procedures. The SDS capillary gel electrophoresis (SDS CGE) method reported herein requires only nanogram-sized proteins loaded onto the autosampler. A sample stacking technique (e.g., head-column field-amplified sample stacking (HC FASS)) was employed, providing three orders of magnitude sensitivity enhancement compared to conventional SDS CGE. This method has been used routinely in purity analysis and characterization of adeno-associated virus (AAV) intermediates and finished gene therapeutics of AAV vectors. The sensitivity achieved is comparable to the currently most sensitive size-based protein assay silver-stained SDS PAGE. The highly sensitive sample stacking SDS CGE can be used for other types of proteins as well.
在过去几十年里,十二烷基硫酸钠聚丙烯酰胺凝胶电泳(SDS-PAGE)一直是基于大小的蛋白质分析的首选方法。然而,一般来说它需要毫克/毫升级别的蛋白质浓度,因此对于痕量水平的蛋白质分析并不实用,更不用说其冗长且 labor-intensive procedures(此处原文有误,推测可能是“labor-intensive procedures”,意为劳动密集型程序)的操作流程了。本文报道的SDS毛细管凝胶电泳(SDS CGE)方法仅需将纳克级大小的蛋白质加载到自动进样器上。采用了一种样品堆积技术(例如,柱头场放大样品堆积(HC FASS)),与传统的SDS CGE相比,灵敏度提高了三个数量级。该方法已常规用于腺相关病毒(AAV)中间体和AAV载体成品基因治疗药物的纯度分析和表征。所实现的灵敏度与目前最灵敏的基于大小的蛋白质分析方法银染SDS PAGE相当。高灵敏度的样品堆积SDS CGE也可用于其他类型的蛋白质。