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:108
|
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
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
相关论文
共 10 条
  • [1] Characterization of Human Serum Albumin isoforms by ion exchange chromatography coupled on-line to native mass spectrometry
    Leblanc, Y.
    Bihoreau, N.
    Chevreux, G.
    JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2018, 1095 : 87 - 93
  • [2] Towards a simple on-line coupling of ion exchange chromatography and native mass spectrometry for the detailed characterization of monoclonal antibodies
    Murisier, Amarande
    Duivelshof, Bastiaan L.
    Fekete, Szabolcs
    Bourquin, Julien
    Schmudlach, Andrew
    Lauber, Matthew A.
    Nguyen, Jennifer M.
    Beck, Alain
    Guillarme, Davy
    D'Atri, Valentina
    JOURNAL OF CHROMATOGRAPHY A, 2021, 1655
  • [3] Multiattribute Monitoring of Antibody Charge Variants by Cation-Exchange Chromatography Coupled to Native Mass Spectrometry
    Haberger, Markus
    Heidenreich, Anna-Katharina
    Hook, Michaela
    Fichtl, Juergen
    Lang, Rainer
    Cymer, Florian
    Adibzadeh, Mandi
    Kuhne, Felix
    Wegele, Harald
    Reusch, Dietmar
    Bonnington, Lea
    Bulau, Patrick
    JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY, 2021, 32 (08) : 2062 - 2071
  • [4] Characterization of Recombinant Monoclonal Antibody Charge Variants Using OFFGEL Fractionation, Weak Anion Exchange Chromatography, and Mass Spectrometry
    Neill, Alyssa
    Nowak, Christine
    Patel, Rekha
    Ponniah, Gomathinayagam
    Gonzalez, Nidia
    Miano, Dino
    Liu, Hongcheng
    ANALYTICAL CHEMISTRY, 2015, 87 (12) : 6204 - 6211
  • [5] On-line characterization of monoclonal antibody variants by liquid chromatography-mass spectrometry operating in a two-dimensional format
    Alvarez, Melissa
    Tremintin, Guillaume
    Wang, Jennifer
    Eng, Marian
    Kao, Yung-Hsiang
    Jeong, Justin
    Ling, Victor T.
    Borisov, Oleg V.
    ANALYTICAL BIOCHEMISTRY, 2011, 419 (01) : 17 - 25
  • [6] Ultrasensitive Characterization of Charge Heterogeneity of Therapeutic Monoclonal Antibodies Using Strong Cation Exchange Chromatography Coupled to Native Mass Spectrometry
    Yan, Yuetian
    Liu, Anita P.
    Wang, Shunhai
    Daly, Thomas J.
    Li, Ning
    ANALYTICAL CHEMISTRY, 2018, 90 (21) : 13013 - 13020
  • [7] Online Collision-Induced Unfolding of Therapeutic Monoclonal Antibody Glyco-Variants through Direct Hyphenation of Cation Exchange Chromatography with Native Ion Mobility-Mass Spectrometry
    van Schaick, Guusje
    Dominguez-Vega, Elena
    Castel, Jerome
    Wuhrer, Manfred
    Hernandez-Alba, Oscar
    Cianferani, Sarah
    ANALYTICAL CHEMISTRY, 2023, 95 (08) : 3932 - 3939
  • [8] Characterization of charge variants, including post-translational modifications and proteoforms, of bispecific antigen-binding protein by cation-exchange chromatography coupled to native mass spectrometry
    Shah, Arnik
    Cui, Weidong
    Harrahy, John
    Ivanov, Alexander R.
    TALANTA, 2024, 266
  • [9] Modeling study of long-term stability of the monoclonal antibody infliximab and biosimilars using liquid-chromatography–tandem mass spectrometry and size-exclusion chromatography–multi-angle light scattering
    Pauline Legrand
    Sophie Dufaÿ
    Nathalie Mignet
    Pascal Houzé
    Rabah Gahoual
    Analytical and Bioanalytical Chemistry, 2023, 415 : 179 - 192
  • [10] Modeling study of long-term stability of the monoclonal antibody infliximab and biosimilars using liquid-chromatography-tandem mass spectrometry and size-exclusion chromatography-multi-angle light scattering
    Legrand, Pauline
    Dufay, Sophie
    Mignet, Nathalie
    Houze, Pascal
    Gahoual, Rabah
    ANALYTICAL AND BIOANALYTICAL CHEMISTRY, 2023, 415 (01) : 179 - 192