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HERO ID
1612620
Reference Type
Journal Article
Title
Host cell protein clearance during protein A chromatography: development of an improved column wash step
Author(s)
Shukla, AA; Hinckley, P
Year
2008
Is Peer Reviewed?
Yes
Journal
Biotechnology Progress
ISSN:
8756-7938
EISSN:
1520-6033
Volume
24
Issue
5
Page Numbers
1115-1121
Language
English
PMID
19194921
DOI
10.1002/btpr.50
Web of Science Id
WOS:000260738900014
Abstract
Host cell protein (HCP) contaminant clearance is a significant concern during downstream process development for biopharmaceuticals. Protein A chromatography as a capture step for monoclonal antibodies and Fc fusion proteins can clear a large proportion of these impurities from cell culture harvest. Nevertheless, remaining levels of this process-related impurity class do present significant constraints on the rapid development of effective and robust polishing steps. Conventionally, an intermediate pH wash is employed between column loading and elution to minimize HCP levels after Protein A chromatography. A significant mechanistic finding presented in this work is that HCP contaminants that persist following Protein A capture predominantly comprise species that associate with the product in preference to direct interaction with the chromatographic resin. This suggests that the development of improved column wash techniques to maximize HCP clearance ought to focus on disrupting protein-HCP interactions rather than Protein A-HCP interactions. A higher wash pH to preserve product--Protein A binding along with the use of additive combinations to disrupt interactions between HCPs and the product are investigated. This strategy was successfully applied to develop a broadly applicable wash condition that has the potential for eliminating the need for product specific optimization of wash conditions. A combination of 1 M urea and 10% isopropanol in the wash buffer were successfully applied as a platform wash condition for Protein A chromatography. Use of this (and other similar) wash conditions are anticipated to aid the rapid development of effective downstream processes for monoclonal antibodies and Fc fusion proteins resulting in their rapid introduction into clinical trials.
Keywords
Protein A chromatography; wash; platform process; host cell protein; monoclonal antibodies
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