Phenylboronic acid as a multi-modal ligand for the capture of monoclonal antibodies: Development and optimization of a washing step

被引:26
作者
dos Santos, Raquel [1 ]
Rosa, Sara A. S. L. [1 ]
Aires-Barros, M. Raquel [1 ]
Tover, Andres [2 ]
Azevedo, Ana M. [1 ]
机构
[1] Univ Lisbon, Ctr Biol & Chem Engn, Inst Super Tecn, Inst Biotechnol & Bioengn,Dept Bioengn, P-1049001 Lisbon, Portugal
[2] Icosagen Cell Factory, EE-61713 Tartumaa, Estonia
关键词
MAbs purification; Multimodal chromatography; Phenylboronate ligands; Capture step; Wash and elution studies; AFFINITY; CHROMATOGRAPHY; PURIFICATION; ADSORPTION; GLYCATION; PROTEINS;
D O I
10.1016/j.chroma.2014.06.001
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
In this work, phenylboronic acid (PBA) was thoroughly investigated as a synthetic ligand for the purification of an immunoglobulin G (IgG) from a clarified cell supernatant from Chinese Hamster Ovary (CHO) cell cultures. In particular, the study was focused on the development of a washing step and in the optimization of the elution step using a serum containing supernatant. From the different conditions tested, best recoveries - 99% - and purifications - protein purity of 81% and a purification factor of 16 out of a maximum of 20 - were achieved using 100 mM D-sorbitol in 10 mM Tris-HCl as washing buffer and 0.5 M D-sorbitol with 150 mM NaCl in 10 mM Tris-HCl as elution buffer. The purification outcome was also compared with protein A chromatography that revealed a recovery of 99%, 87% protein purity and 29 out of a maximum of 33 purification factor. Following the main purification, purified IgG was characterized in terms of isoelectric point, size and activity. In the end, a proof of concept was performed using two different mAbs from serum-free CHO cell cultures. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:115 / 124
页数:10
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