Adsorption of peptides and small proteins with control access polymer permeation to affinity binding sites. Part I: Polymer permeation-immobilized metal ion affinity chromatography separation adsorbents with polyethylene glycol and immobilized metal ions
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Despite the many efforts to develop efficient protein purification techniques, the isolation of peptides and small proteins on a larger than analytical scale remains a significant challenge. Recovery of small biomolecules from diluted complex biological mixtures, such as human serum, employing porous adsorbents is a difficult task mainly due to the presence of concentrated large biomolecules that can add undesired effects in the system such as blocking of adsorbent pores, impairing diffusion of small molecules, or competition for adsorption sites. Adsorption and size exclusion chromatography (AdSEC) controlled access media, using polyethylene glycol (PEG) as a semi-permeable barrier on a polysaccharide matrix, have been developed and explored in this work to overcome such effects and to preferentially adsorb small molecules while rejecting large ones. In the first part of this work, adsorption studies were performed with small peptides and proteins from synthetic mixtures using controlled access polymer permeation adsorption (CAPPA) media created by effectively grafting PEG on an immobilized metal affinity chromatography (IMAC) agarose resin, where chelating agents and immobilized metal ions were used as the primary affinity binding sites. Synthetic mixtures consisted of bovine serum albumin (BSA) with small proteins, peptides, amino acids (such as histidine or Val 4-Angiotensin III), and small molecules-spiked human serum. The synthesized hybrid adsorbent consisted of agarose beads modified with iminodiacetic (IDA) groups, loaded with immobilized Cu(II) ions, and PEG. These CAPPA media with grafted PEG on the interior and exterior surfaces of the agarose matrix were effective in rejecting high molecular weight proteins. Different PEG grafting densities and PEG of different molecular weight were tested to determine their effect in rejecting and controlling adsorbent permeation properties. Low grafting density of high molecular weight PEG was found to be as effective as high grafting density of low molecular weight PEG in the rejecting properties of the semi-permeable synthesized media. © 2012 Elsevier B.V.
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Adsorption; Bioseparations; Chromatography; IMAC; Polyethylene glycol; RAM Adsorption site; Adsorption studies; Affinity binding; Agarose; Agarose beads; Angiotensin III; Bio separation; Biological mixtures; Bovine serum albumins; Chelating agent; Control access; Exterior surfaces; Grafting densities; High molecular weight; High molecular weight protein; Human serum; Hybrid adsorbents; IMAC; Immobilized metal affinity chromatography; Immobilized metals; Large biomolecules; Low molecular weight; matrix; Metal-ion affinity chromatography; Permeation properties; Polysaccharide matrix; Porous adsorbent; Protein purification; Small molecules; Synthetic mixtures; Access control; Adsorbents; Adsorption; Affinity chromatography; Amino acids; Biomolecules; Body fluids; Chelation; Chromatography; Grafting (chemical); Metal ions; Mixtures; Molecular weight; Molecules; Peptides; Polyethylene oxides; Polymers; Random access storage; Size exclusion chromatography; Polyethylene glycols; adsorbent; agarose; angiotensin III; bovine serum albumin; chelating agent; copper ion; histidine; macrogol; metal ion; polymer; polysaccharide; resin; adsorption chromatography; adsorption kinetics; article; binding affinity; binding site; concentration (parameters); controlled study; desorption; gel permeation chromatography; human; immobilized metal affinity chromatography; molecular weight; peptide analysis; priority journal; Adsorption; Animals; Cattle; Chromatography, Affinity; Chromatography, Gel; Copper; Humans; Models, Chemical; Peptides; Polyethylene Glycols; Proteins; Bovinae
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