Application of the Protein Maker as a platform purification system for therapeutic antibody research and development

被引:7
作者
Helie, Genevieve [1 ]
Parat, Marie [1 ]
Masse, Frederic [2 ]
Gerdts, Cory J. [3 ]
Loisel, Thomas P. [1 ]
Matte, Allan [1 ]
机构
[1] Natl Res Council Canada, Prot Purificat Human Hlth Therapeut, 6100 Royalmount Ave, Montreal, PQ H4P 2R2, Canada
[2] Natl Res Council Canada, Primary Assays Human Hlth Therapeut, 6100 Royalmount Ave, Montreal, PQ H4P 2R2, Canada
[3] Prot BioSolut Inc, Suite 280,401 Profess Dr, Gaithersburg, MD 20879 USA
关键词
Parallelized protein purification; Antibody; Protein A; Protein G; Hybridoma; Process development; HIGH-THROUGHPUT PURIFICATION; MONOCLONAL-ANTIBODIES; A CHROMATOGRAPHY; EXCHANGE;
D O I
10.1016/j.csbj.2016.06.001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Within the research and development environment, higher throughput, parallelized protein purification is required for numerous activities, from small scale purification of monoclonal antibodies (mAbs) and antibody fragments for in vitro and in vivo assays to process development and optimization for manufacturing. Here, we describe specific applications and associated workflows of the Protein Maker liquid handling system utilized in both of these contexts. To meet the requirements for various in vitro assays, for the identification and validation of new therapeutic targets, small quantities of large numbers of purified antibodies or antibody fragments are often required. Reducing host cell proteins (HCP) levels following capture with Protein A by evaluating various wash buffers is an example of how parallelized protein purification can be leveraged to improve a process development outcome. Stability testing under various conditions of in-process intermediates, as an example, the mAb product from a clarified harvest, requires parallelized protein purification to generate concurrent samples for downstream assays. We have found that the Protein Maker can be successfully utilized for small-to-mid scale platform purification or for process development applications to generate the necessary purified protein samples. The ability to purify and buffer exchange up to 24 samples in parallel offers a significant reduction in time and cost per sample compared to serial purification using a traditional FPLC system. By combining the Protein Maker purification system with a TECAN Freedom EVO liquid handler for automated buffer exchange we have created a new, integrated platform for a variety of protein purification and process development applications. Crown Copyright (C) 2016 Published by Elsevier B.V. on behalf of Research Network of Computational and Structural Biotechnology.
引用
收藏
页码:238 / 244
页数:7
相关论文
共 18 条
[1]   A Novel Approach to Monitor Clearance of Host Cell Proteins Associated With Monoclonal Antibodies [J].
Aboulaich, Nabila ;
Chung, Wai Keen ;
Thompson, Jenny Heidbrink ;
Larkin, Christopher ;
Robbins, David ;
Zhu, Min .
BIOTECHNOLOGY PROGRESS, 2014, 30 (05) :1114-1124
[2]  
Alm Tove, 2007, Biotechnology Journal, V2, P709, DOI 10.1002/biot.200700060
[3]   Development of robust antibody purification by optimizing protein-A chromatography in combination with precipitation methodologies [J].
Chollangi, Srinivas ;
Parker, Ray ;
Singh, Nripen ;
Li, Yi ;
Borys, Michael ;
Li, Zhengjian .
BIOTECHNOLOGY AND BIOENGINEERING, 2015, 112 (11) :2292-2304
[4]   A simple high-throughput purification method for hit identification in protein screening [J].
Cummins, Emma ;
Luxenberg, Deborah P. ;
McAleese, Fionnuala ;
Widom, Angela ;
Fennell, Brian J. ;
Darmanin-Sheehan, Alfredo ;
Whitters, Matthew J. ;
Bloom, Laird ;
Gill, Davinder ;
Cunningham, Orla .
JOURNAL OF IMMUNOLOGICAL METHODS, 2008, 339 (01) :38-46
[5]   Screening the mammalian extracellular proteome for regulators of embryonic human stem cell pluripotency [J].
Gonzalez, Rodolfo ;
Jennings, Lori L. ;
Knuth, Mark ;
Orth, Anthony P. ;
Klock, Heath E. ;
Ou, Weija ;
Feuerhelm, Julie ;
Hull, Mitchell V. ;
Koesema, Eric ;
Wang, Yuping ;
Zhang, Jia ;
Wu, Chunlei ;
Cho, Charles Y. ;
Su, Andrew I. ;
Batalov, Serge ;
Chen, Hong ;
Johnson, Kristen ;
Laffitte, Bryan ;
Nguyen, Deborah G. ;
Snyder, Evan Y. ;
Schultz, Peter G. ;
Harris, Jennifer L. ;
Lesley, Scott A. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2010, 107 (08) :3552-3557
[6]   REMOVAL OF SIALIC-ACID FROM A GLYCOPROTEIN IN CHO CELL-CULTURE SUPERNATANT BY ACTION OF AN EXTRACELLULAR CHO CELL SIALIDASE [J].
GRAMER, MJ ;
GOOCHEE, CF ;
CHOCK, VY ;
BROUSSEAU, DT ;
SLIWKOWSKI, MB .
BIO-TECHNOLOGY, 1995, 13 (07) :692-698
[7]   Automated harvesting and 2-step purification of unclarified mammalian cell-culture broths containing antibodies [J].
Holenstein, Fabian ;
Eriksson, Christer ;
Erlandsson, Ioana ;
Norrman, Nils ;
Simon, Jill ;
Danielsson, Ake ;
Milicov, Adriana ;
Schindler, Patrick ;
Schlaeppi, Jean-Marc .
JOURNAL OF CHROMATOGRAPHY A, 2015, 1418 :103-109
[8]   High-throughput screening of chromatographic separations: IV. Ion-exchange [J].
Kelley, Brian D. ;
Switzer, Mary ;
Bastek, Patrick ;
Kramarczyk, Jack F. ;
Molnar, Kathleen ;
Yu, Tianning ;
Coffman, Jon .
BIOTECHNOLOGY AND BIOENGINEERING, 2008, 100 (05) :950-963
[9]   A semi-automated method for purification of milligram quantities of proteins on the QIAcube [J].
McGraw, J. ;
Tatipelli, V. K. ;
Feyijinmi, O. ;
Traore, M. C. ;
Eangoor, P. ;
Lane, S. ;
Stollar, E. J. .
PROTEIN EXPRESSION AND PURIFICATION, 2014, 96 :48-53
[10]   Production of α2,6-sialylated IgG1 in CHO cells [J].
Raymond, Celine ;
Robotham, Anna ;
Spearman, Maureen ;
Butler, Michael ;
Kelly, John ;
Durocher, Yves .
MABS, 2015, 7 (03) :571-583