Abstract
Abstract High performance liquid affinity chromatography (HPLAC) is a powerful method for purification and analysis of biological compounds. It combines the speed and the efficiency of high performance chromatography with the selectivity of affinity chromatography methods. The selectivity depends, first, on the nature of the ligand used; this latter must exhibit a specific binding affinity towards the product to purify; second, it depends on adsorption and desorption processus that improve, or not, the protein affinity for the ligand. The presence of N-acetyl neuraminic acid surrounding the insulin receptor structure shows that this acid may develop specific interactions with insulin. We performed the grafting of sialic acid on coated silica supports. The performances of these supports towards insulin were studied by HPLAC. The ligand specificity was tested in presence of two forms of insulin, porcine and bovine insulins, which, differ from each other by only two amino acids in their structure. The suppor...
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More From: Journal of Liquid Chromatography & Related Technologies
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