| Popis: |
Novel immobilized metal affinity membrane adsorbers (IMA-MA) were studied for potential use as stationary phases for protein separation. Protein adsorption on IMA-MA loaded with Cu(II), Ni(II), ZN(II) and Co(II) ions was compared as a function of the flow-rate and the ionic strength of the elution buffer. To exclude the possibility of mixed-mode interaction in the experiments, the binding of proteins similar in terms of hydrophobicity, isoelectric point, size and mass-to-charge ratio but differing in their number of surface histidine residues was investigated. Matrix-assisted laser desorption/ionization mass spectrometry was used to distinguish between these proteins in the eluted fractions. Salt concentration of at least 0.5 M NACl and flow-rates below 2 ml min−1 were found suitable to ensure an adsorption mechanism based on affinity interaction between the proteins and the chelated metal ions. In an application study, the IMA-MA and conventional chelating Sepharose fast flow columns were compared for the isolation of a recombinant fusion protein (EcoR V), which carried a polyhistidine sequence (HIS6-tag) at the N-terminus. |
