Artikel: De novo discovery of peptide-based affinity ligands for the fab fragment of human immunoglobulin G
Journal of chromatography. 2022 Apr. 26, v. 1669
2022
Abstract: Antibody fragments and their engineered variants show true potential as next-generation therapeutics as they combine excellent targeting with superior biodistribution and blood clearance. Unlike full antibodies, however, antibody fragments do not yet ... ...
Abstract | Antibody fragments and their engineered variants show true potential as next-generation therapeutics as they combine excellent targeting with superior biodistribution and blood clearance. Unlike full antibodies, however, antibody fragments do not yet have a standard platform purification process for large-scale production. Short peptide ligands are viable alternatives to protein ligands in affinity chromatography. In this work, an integrated computational and experimental scheme is described to de novo design 9-mer peptides that bind to Fab fragments. The first cohort of designed sequences was tested experimentally using human polyclonal Fab, and the top performing sequence was selected as a prototype for a subsequent round of ligand refinement in silico. The resulting peptides were conjugated to chromatographic resins and evaluated via equilibrium and dynamic binding studies using human Fab-κ and Fab-λ. The equilibrium studies returned values of binding capacities up to 32 mg of Fab per mL of resin with mild affinity (KD ∼ 10⁻⁵ M) that are conducive to high product capture and recovery. Dynamic studies returned values of product yield up to ∼90%. Preliminary purification studies provided purities of 83–93% and yields of 11–89%. These results lay the groundwork for future development of these ligands towards biomanufacturing translation. |
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Schlagwörter | affinity chromatography ; antibodies ; blood ; computer simulation ; humans ; immunoglobulin G ; ligands ; peptides ; prototypes ; purification methods ; therapeutics |
Sprache | Englisch |
Erscheinungsverlauf | 2022-0426 |
Erscheinungsort | Elsevier B.V. |
Dokumenttyp | Artikel |
ZDB-ID | 218139-3 |
ISSN | 0021-9673 ; 0378-4355 ; 0376-737X |
ISSN | 0021-9673 ; 0378-4355 ; 0376-737X |
DOI | 10.1016/j.chroma.2022.462941 |
Datenquelle | NAL Katalog (AGRICOLA) |
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