Charge variants characterization of a monoclonal antibody by ion exchange chromatography coupled on-line to native mass spectrometry: Case study after a long-term storage at+5 °C

被引:110
作者
Leblanc, Y. [1 ]
Ramon, C. [1 ]
Bihoreau, N. [1 ]
Chevreux, G. [1 ]
机构
[1] LFB Biotechnol, 3 Ave Tropiques, F-91958 Les Ulis, France
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2017年 / 1048卷
关键词
Mass spectrometry; Ion exchange chromatography; IdeS; Deamidation; Monoclonal antibody; Charge variants; LIQUID-CHROMATOGRAPHY; METHIONINE OXIDATION; LC-MS; DEAMIDATION RATES; ANION-EXCHANGE; HEAVY-CHAIN; PROTEIN-A; HETEROGENEITY; IGG1; IDENTIFICATION;
D O I
10.1016/j.jchromb.2017.02.017
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Numerous putative post-translational modifications may induce variations of monoclonal antibodies charge distribution that can potentially affect their biological activity. The characterization and the monitoring of these charge variants are critical quality requirements to ensure stability and process consistency. Charge variants are usually characterized by preparative ion exchange chromatography, collection of fractions and subsequent reverse-phase liquid chromatography with mass spectrometry analysis. While this process can be automatized by on-line two-dimensional chromatography, it remains often complex and time consuming. For this reason, a straightforward on-line charge variant analysis method is highly desirable and analytical laboratories are actively pursuing efforts to overcome this challenge. In this study, a mixed mode ion exchange chromatographic method using volatile salts and coupled online to native mass spectrometry was developed in association with a middle-up approach for a detailed characterization of monoclonal antibodies charge variants. An aged monoclonal antibody, presenting a complex charge variant profile was successfully investigated by this methodology as a case study. Results demonstrate that deamidation of the heavy chain was the major degradation pathway after long-term storage at 5 degrees C while oxidation was rather low. The method was also very useful to identify all the clipped forms of the antibody. (C) 2017 LFB Biotechnologies. Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND license
引用
收藏
页码:130 / 139
页数:10
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