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Directed evolution generated multivalent ligands for the HIV antibody, 2G12. A selection among ∼1013 neo-glycopeptides, prepared through cell-free ribosomal translation and chemical glycosylation, yielded high-avidity glycopeptides with 3–4 oligomannose residues, matching the number of binding sites in the dimeric 2G12 (adapted from Horiya et al. 2014). This figure is available in black and white in print and in color at Glycobiology online.
