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Updated: Jun 25, 2026

Ion Exchange Chromatography (IEX) Coupled to Multi-angle Light Scattering (MALS) for Protein Separation and Characterization
Published on: April 5, 2019
Theoretical background of monolithic short layer ion-exchange chromatography for separation of charged large
Shuichi Yamamoto1, Noriko Yoshimoto, Yukiko Nishizumi
1Bio-Process Engineering Laboratory, School of Engineering and Graduate School of Medicine, Yamaguchi University, Tokiwadai, Ube 755-8611, Japan. shuichi@yamaguchi-u.ac.jp
Abstract:
The retention and peak spreading in linear gradient elution of charged large biomolecules were investigated by using numerical simulations. Oligo-DNA separation by monolithic anion-exchange chromatography was chosen as a model system. The peak width and the retention were well predicted by using the parameters obtained by gradient elution experiments at different gradient slopes. As the distribution coefficient at the peak retention volume K(R) decreases with increasing molecular size, the peak became sharper for larger DNAs. This is due to very large effective charge (binding site) values of large DNAs (20-60). The peak width was well correlated with K(R) based on the model equation developed for linear gradient elution of proteins. It was shown that the monolithic disk is best suited for very large charged biomolecule separations at high flow velocities with shallow gradients slopes.
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