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GE Healthcare Life Sciences Part of GE Healthcare
Education Centre
About the purification of biomolecules
Purpose of purification
Developing purification protocols
How to combine purification steps
Purification development - summary
LC techniques
Affinity Chromatography
Desalting & Gel Filtration
Hydrophobic interaction chromatography
Ion exchange chromatography
Animation
Basic Principles
The Separation Mechanism
Type of ion exchangers
Elution modes
The typical Ion exchange experiment
Charge properties of proteins and peptides
Effect of running pH
Resolution in IEX
Optimisation of IEX experiments
Ion Exchange in practice
Technique Profile
What is Ion Exchange?
Reversed phase chromatography
Protein Purifier software
BioProcess™ Glossary

Resolution in ion exchange chromatography

    For a detailed discussion on zone broadening and resolution in general, see
    Basic Principles in Gel Filtration: 5. Resolution in gel filtration.

    In IEX, selectivity (distance between and order of eluted peaks) depends on the charge properties of the individual sample components.
    With proteins and peptides the charge properties are heavily influenced by the running pH.
    Gradients will influence peak-spacing but not elution order.

    Efficiency (counteraction of zone broadening) depends on bead size, quality of the packed bed and flow rate in isocratic and gradient modes.

    Best resolution is theoretically obtained in isocratic mode.
    For practical reasons, however, gradient mode is the most frequently used elution technique.

    With large volumes of complex samples, the first purification step often aims at concentrating the sample and removing the bulk of the contaminants by a capture step. Here, step elution mode is to be preferred because of its high loading capacity and that high flow rates can be applied.