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Development of peptide affinity ligands for the purification of polyclonal and monoclonal Fabs from recombinant fluids

J Chromatogr A. 2022; 
Ryan Kilgore, Wenning Chu, Dipendra Bhandari, David Fischler, Ruben G Carbonell, Michael Crapanzano, Stefano Menegatti
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Proteins, Expression, Isolation and Analysis … The dynamic binding capacity of Capto L and GenScript Protein L Resin was measured via continuous loading of human polyclonal Fab at 1 mg/mL in PBS at the linear velocity of either … Get A Quote

摘要

Engineered multi-specific monoclonal antibodies (msAbs) and antibody fragments offer valuable therapeutic options against metabolic disorders, aggressive cancers, and viral infections. The advancement in molecular design and recombinant expression of these next-generation drugs, however, is not equaled by the progress in downstream bioprocess technology. The purification of msAbs and fragments requires affinity adsorbents with orthogonal biorecognition of different portions of the antibody structure, namely its Fc (fragment crystallizable) and Fab (fragment antigen-binding) regions or the C1-3 and C chains. Current adsorbents rely on protein ligands that, while featuring high binding capacity and selectivity, n... More

關鍵詞

Affinity chromatography, Cell culture harvests, Fragment antigen binding, Monoclonal antibodies, Peptide ligands
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