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• W2162862954 abstract "This work describes the assessment of a de novo synthetic affinity ligand for recombinant human erythropoietin (rHuEPO), based on the multicomponent Ugi reaction. Four Ugi ligands were designed based on the X-ray crystallographic structure of the complex between human erythropoietin and site 1 of its cell-surface receptor (EPObp)2 ; screening of the ligands with pure rHuEPO samples identified a lead ligand (A9C10I8) immobilized on aldehyde-functionalized agarose beads, which was able to bind and elute erythropoietin, as determined by SDS-PAGE and Western blot analyses. Furthermore, small-scale affinity chromatography performed on the immobilized adsorbent showed its ability to isolate rHuEPO from a spiked mammalian cell supernatant with a purity of ∼80%, as estimated with gel densitometry. This approach could lead to the development of a cost-effective downstream process for rHuEPO, as an alternative to the current multi-step purification protocols." @default.
• W2162862954 created "2016-06-24" @default.
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• W2162862954 date "2013-05-16" @default.
• W2162862954 modified "2023-10-16" @default.
• W2162862954 title "Design, synthesis, and assessment of a de novo affinity adsorbent for the purification of recombinant human erythropoietin" @default.
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• W2162862954 doi "https://doi.org/10.1002/bit.24943" @default.
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