On-line characterization of monoclonal antibody variants by liquid chromatography-mass spectrometry operating in a two-dimensional format

被引:84
作者
Alvarez, Melissa [1 ]
Tremintin, Guillaume [2 ]
Wang, Jennifer [1 ]
Eng, Marian [1 ]
Kao, Yung-Hsiang [1 ]
Jeong, Justin [1 ]
Ling, Victor T. [1 ]
Borisov, Oleg V. [1 ]
机构
[1] Genentech Inc, Prot Analyt Chem, San Francisco, CA 94080 USA
[2] Dionex, Sunnyvale, CA 94085 USA
关键词
Mass spectrometry; Liquid chromatography-mass spectrometry; Monoclonal antibodies; Variants; Ion exchange chromatography; Size exclusion chromatography; Two-dimensional liquid chromatography; RECOMBINANT; GLYCOSYLATION; HETEROGENEITY; IDENTIFICATION; AGGREGATION; SEPARATION; PRODUCTS; HPLC;
D O I
10.1016/j.ab.2011.07.033
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Recombinant monoclonal antibodies (MAbs) have become one of the most rapidly growing classes of biotherapeutics in the treatment of human disease. MAbs are highly heterogeneous proteins, thereby requiring a battery of analytical technologies for their characterization. However, incompatibility between separation and subsequent detection is often encountered. Here we demonstrate the utility of a generic on-line liquid chromatography-mass spectrometry (LC-MS) method operated in a two-dimensional format toward the rapid characterization of MAb charge and size variants. Using a single chromatographic system capable of running two independent gradients, up to six fractions of interest from an ion exchange (IEC) or size exclusion (SEC) separation can be identified by trapping and desalting the fractions onto a series of reversed phase trap cartridges with subsequent on-line analysis by mass spectrometry. Analysis of poorly resolved and low-level peaks in the IEC or SEC profile was facilitated by preconcentrating fractions on the traps using multiple injections. An on-line disulfide reduction step was successfully incorporated into the workflow, allowing more detailed characterization of modified MAbs by providing chain-specific information. The system is fully automated, thereby enabling high-throughput analysis with minimal sample handling. This technology provides rapid data turnaround time, a much needed feature during product characterization and development of multiple biotherapeutic proteins. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:17 / 25
页数:9
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