Resin structure impacts two-component protein adsorption and separation in anion exchange chromatography

• Published in: Journal of Chromatography A 2023-08, Vol.1705, p.464208, Article 464208
• Main Authors: Beck, Jürgen, Hochdaninger, Georg, Carta, Giorgio, Hahn, Rainer
• Format: Article
• Language: English
• Subjects: Batch adsorption; CLSM; Frontal chromatography; Mass transfer
• ISSN: 0021-9673
• DOI: 10.1016/j.chroma.2023.464208

•Protein separation during loading can be achieved on macro-porous resins.•Resin structure determines separation efficiency.•Polymer grafts inhibit diffusion of displaced protein.•High binding capacity is not the only criterium for choosing a resin for a process. The influence of the resin structure, on the competitive binding and separation of a two-component protein mixture with anion exchange resins is evaluated using conalbumin and green fluorescent protein as a model system. Two macroporous resins, one with large open pores and one with smaller pores, are compared to a resin with grafted polymers. Investigations include measurements of single and two-component isotherms, batch uptake kinetics and two-component column breakthrough. On both macroporous resins, the weaker binding protein, conalbumin, is displaced by the stronger binding green fluorescent protein. For the large pore resin, this results in a pronounced overshoot and efficient separation by frontal chromatography. The polymer-grafted resin exhibits superior capacity and kinetics for one-component adsorption, but is unable to achieve separation due to strongly hindered counter-diffusion. Intermediate separation efficiency is obtained with the smaller pore resin. Confocal laser scanning microscopy provides a mechanistic explanation of the underlying intra-particle diffusional phenomena revealing whether unhindered counter-diffusion of the displaced protein can occur or not. This study demonstrates that the resin's intra-particle structure and its effects on diffusional transport are crucial for an efficient separation process. The novelty of this work lies in its comprehensive nature which includes examples of the three most commonly used resin structures: a small pore agarose matrix, a large-pore polymeric matrix, and a polymer grafted resin. Comparison of the protein adsorption properties of these materials provides valuable clues about advantages and disadvantages of each for anion exchange chromatography applications.