Biotechnology and Bioengineering · 1989 · 84 citations · 9 references
Life SciencesBiochemistryBioengineeringBiomaterialsEnzymologyPolymer ChemistryEnzyme InhibitionLigand BindingPolymer FunctionalizationPolymerization ChemistryProtein ChemistryProteolytic EnzymesAffinity ImmobilizationImmobilizationLigand ImmobilizationProtein ImmobilizationProtein Purification By AdsorptionProtein-based MaterialsProtein-based Polymers
Reactive polymers have been prepared by copolymeriz-ing N-isopropyl acrylamide (NIPAM) with N-acryloxy-succinimide (NASI) or glycidyl methacrylate (GMA). The amino groups of ligands could react with the residues of NASI or GMA and the polymers could be precipitated by temperature and/or salinity variation, since they contained the NIPAM residues. As a model, p-aminobenza-midine, a trypsin inhibitor, was attached to the polymers to form water-soluble macroligands, capable of selectively binding trypsin from a trypsin-chymotrypsin solution. After precipitation of the macroligand-trypsin complex, followed by dissociation, approximately 82% trypsin was isolated. The NIPAM-GMA copolymer was also reacted with immunogammaglobulin (IgG) and alkaline phosphatase (AP). It was demonstrated that the IgG bearing polymer was able to bind protein A and the whole complex was precipitable. The reactive polymer was also used for direct immobilization of AP which was active in repeated reactions.
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Protein A: nature's universal anti-antibody
Avadhesha Surolia, Debkumar Pain, M.I. Khan · Trends in Biochemical Sciences · 1982 · 110 citations
Ultrafiltration affinity purification
Bo Mattìasson, Matts Ramstorp · Journal of Chromatography A · 1984 · 57 citations