“…Frequently, affinity chromatography has been employed as the preferred separation method at the laboratory or process scale [13] with the traditional ligands based on bacterial Fc receptors, such as Protein A from Staphylococcus aureus, or Protein G from Streptococcus sp, favoured [5,14,15]. The use of such biological ligands, however, has several drawbacks including their overall low productivity [12] and their relatively high cost [13]. In addition, the low pH conditions required to elute the antibody from Protein A resins can damage both the target and ligand proteins and can be incompatible with subsequent downstream steps [12,16].…”