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Affinity chromatography Chromatography media 4 Technique description Affinity chromatography The inherent high specificity of ligand – target interactions makes affinity chromatography particularly suitable for the Capture stage of downstream processing. One of the typical advantages of using affinity techniques is that the capacity of the media is usually not affected by the presence of contaminants since they have no affinity for the coupled ligand. The result is reliable product purity, often with purification factors well over 1000, and effective concentration, achieved in a single step. Affinity chromatography may also be suitable for the Intermediate or Polishing stages, to remove small amounts of specific contaminants. In affinity chromatography, the product to be purified adsorbs to an affinity ligand that is coupled to a matrix. The ligand is specific for a single type of protein/ peptide molecule, or group of such molecules. The targeted product often binds to the ligand under specific conditions of ionic strength and pH. After unbound impurities are rinsed away, the product can be eluted by using a step gradient of increasing or decreasing ionic strength and/ or by changing the pH, or by a more selective elution technique. The most widely used affinity chromatography purification step today is the capture of antibodies using the Protein A ligand. Protein A media The MabSelect family for the capture of monoclonal antibodies has been developed with industrial needs in mind. The expanded product range focuses on better overall process economy and reduced time for optimization. Group-specific media Heparin Sepharose 6 Fast Flow and Blue Sepharose 6 Fast Flow are examples of media with affinity for a group of related molecules. IMAC media Immobilized Metal Ion Chromatography (IMAC) is a versatile purification technique for proteins, including histidine-tagged proteins, with an affinity for metal ions. Ni Sepharose 6 Fast Flow is precharged with Ni2+ ions and is designed for purification of histidine-tagged proteins, suitable for scale-up and accompanied with a Regulatory Support File. IMAC Sepharose 6 Fast Flow is the uncharged version (with the possibility to charge the metal ion of your choice), suitable for histidine-tagged proteins as well as other recombinant proteins and native proteins. Chelating Sepharose Fast Flow is the well-established BioProcess IMAC medium and is being used in several approved biopharmaceutical process. Pre-activated media Pre-activated media allow you to couple a ligand appropriate to your application. The choice of medium depends on several factors, for example the groups in the ligand molecule that are suitable for coupling and the chemical stability demands on the resulting affinity medium. CNBr-activated Sepharose 4 Fast Flow and NHSactivated Sepharose 4 Fast Flow are examples of modern pre-activated media suitable for attaching various ligands. 70 www.gelifesciences.com/bioprocess