The effect of kosmotropic salts on aggregate removal from monoclonal antibodies in mixed-mode anion exchange chromatography

被引:4
作者
Konrad, Susanne [1 ]
Graf, Tobias [1 ]
Falkenstein, Roberto [1 ]
机构
[1] Roche Diagnost GmbH, Nonnenwald 2, D-82377 Penzberg, Germany
关键词
Kosmotropic salts; high molecular weight impurities; Hydrophobicity; Mixed mode chromatography; monoclonal antibody purification; HYDROPHOBIC INTERACTION CHROMATOGRAPHY; PURIFICATION; SELECTIVITY; SEPARATION; CLEARANCE; PROTEINS; QUALITY; DESIGN;
D O I
10.1016/j.crbiot.2023.100139
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Efficacious and safe application of recombinant proteins in humans as drugs depends on their high purity accomplished by downstream processing. The present study evaluates the effects of kosmotropic salts used in the flow-through mode of mixed-mode anion exchange (MMAEX) chromatography to remove high molecular weight (HMW) impurities efficiently from monoclonal antibody (mAb) products. For this purpose, the impact of different kosmotropic salts at varying concentrations along with changes of the pH were systematically assessed by high throughput screens on a set of mAbs differing in their relative hydrophobicity. In contrast to the more hydrophobic mAbs, for the more hydrophilic mAbs, a clear and consistent removal of HMW species to values > 80% (achieving up to 2.5-fold improvement) occurred with the addition of increasing amounts of a kosmotropic salt (sodium chloride, sodium sulfate, ammonium sulfate, potassium chloride and potassium sulfate) to the loads applied to MMAEX chromatography. Overall, the herein described effect on the removal of HMW species by MMAEX resins was specific for kosmotropic salts, independent of conductivity, and facilitated by slightly basic pH conditions. These findings were confirmed at lab-scale operation achieving > 99% purity, indicating the potential to implement MMAEX in combination with kosmotropic salts as a polishing step for hydrophilic mAbs.
引用
收藏
页数:11
相关论文
共 41 条
[1]  
Ajayi O., 2021, ANAL VIRAL CLEARANCE
[2]   An updated analysis of viral clearance unit operations for biotechnology manufacturing [J].
Ajayi, Opeyemi O. ;
Johnson, Sarah A. ;
Faison, Talia ;
Azer, Nicole ;
Cullinan, Jackie L. ;
Dement-Brown, Jessica ;
Lute, Scott C. .
CURRENT RESEARCH IN BIOTECHNOLOGY, 2022, 4 :190-202
[3]   Hydrophobic interaction chromatography as polishing step enables obtaining ultra-pure recombinant antibodies [J].
Antunes Pereira Bresolin, Iara Rocha ;
Lingg, Nico ;
Lazzarotto Bresolin, Igor Tadeu ;
Jungbauer, Alois .
JOURNAL OF BIOTECHNOLOGY, 2020, 324
[4]   The Immunogenicity of Antibody Aggregates in a Novel Transgenic Mouse Model [J].
Bessa, Juliana ;
Boeckle, Sabine ;
Beck, Hermann ;
Buckel, Thomas ;
Schlicht, Sonja ;
Ebeling, Martin ;
Kiialainen, Anna ;
Koulov, Atanas ;
Boll, Bjorn ;
Weiser, Thomas ;
Singer, Thomas ;
Rolink, Antonius G. ;
Iglesias, Antonio .
PHARMACEUTICAL RESEARCH, 2015, 32 (07) :2344-2359
[5]   The Role of Ligand-Ligand Interactions in Multimodal Ligand Conformational Equilibria and Surface Pattern Formation [J].
Bilodeau, Camille L. ;
Lau, Edmond Y. ;
Cramer, Steven M. ;
Garde, Shekhar .
LANGMUIR, 2020, 36 (31) :9054-9063
[6]   Formation of Ligand Clusters on Multimodal Chromatographic Surfaces [J].
Bilodeau, Camille L. ;
Lau, Edmond Y. ;
Roush, David ;
Garde, Shekhar ;
Cramer, Steven M. .
LANGMUIR, 2019, 35 (51) :16770-16779
[7]   Prediction of Aggregation Prone Regions of Therapeutic Proteins [J].
Chennamsetty, Naresh ;
Voynov, Vladimir ;
Kayser, Veysel ;
Helk, Bernhard ;
Trout, Bernhardt L. .
JOURNAL OF PHYSICAL CHEMISTRY B, 2010, 114 (19) :6614-6624
[8]   Purification of antibody Fab and F(ab′)2 fragments using Gradiflow technologyl [J].
Cheung, GLM ;
Thomas, TM ;
Rylatt, DB .
PROTEIN EXPRESSION AND PURIFICATION, 2003, 32 (01) :135-140
[9]   Resolution of heterogeneous charged antibody aggregates via multimodal chromatography: A comparison to conventional approaches [J].
Chmielowski, Rebecca A. ;
Meissner, Sandra ;
Roush, David ;
Linden, Thomas O. ;
Glowacki, Edward ;
Konietzko, Janelle ;
Nti-Gyabaah, Joseph .
BIOTECHNOLOGY PROGRESS, 2014, 30 (03) :636-645
[10]   Using high throughput screening to define virus clearance by chromatography resins [J].
Connell-Crowley, Lisa ;
Larimore, Elizabeth A. ;
Gillespie, Ron .
BIOTECHNOLOGY AND BIOENGINEERING, 2013, 110 (07) :1984-1994