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Updated: Aug 5, 2026

Isolation and Characterization Of Chimeric Human Fc-expressing Proteins Using Protein A Membrane Adsorbers And A Streamlined Workflow
Published on: January 8, 2014
Advantages of Protein A Membrane Chromatography: High Productivity, Strong Impurity Removal Capability, and More
Yifeng Li1, Hang Zhou2, Sherry Gu3
1Downstream Process Development (DSPD), WuXi Biologics, 31 Yiwei Road, Waigaoqiao Free Trade Zone, Shanghai 200131, China.
Abstract:
Protein A affinity chromatography is the gold standard for antibody purification. In practice, it is mainly performed using resin-based packed bed columns. However, for porous resins, mass transport depends on slow diffusion and, consequently, low flow rates/long residence times are required to achieve decent binding capacities (i.e., >30 mg/mL), which leads to long processing time and low productivity. Recently, Protein A membranes have emerged as a promising alternative to Protein A columns. Membrane adsorbers, which have large pores, enable convection-based mass transport and allow high dynamic binding capacity to be achieved at a relatively short residence time (on the order of seconds). Hence, Protein A membranes can be operated at high flow rates and gain significantly improved productivity. In addition to high productivity, we recently found that Protein A membranes possess a much stronger impurity-removing capability than Protein A columns. This review introduces the advantages that Protein A membrane chromatography offers, especially those that have not been well recognized before. These advantages allow high-quality products to be obtained with significantly reduced costs.
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