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. 2021 Jul 12;95(15):e02350-20. doi: 10.1128/JVI.02350-20

FIG 2.

FIG 2

Recombination of known beneficial CDR sequences to engineer novel D5 variants. (A) Mutated CDR sequences of four highlighted D5 variants reported by Montgomery et al. (67) aligned with the wild-type (WT) sequence. These mutated CDR sequences were used to engineer the 11 recombined variants. (B) Left, paratope map of the binding sites for D5 Fab with its antigen, 5-helix. NHR, yellow; CHR, light blue. Areas of contact with the D5 CDR loops are represented as VH CDR1 (red), VH CDR2 (green), VH CDR3 (magenta), and VL CDR3 (blue). Right, X-ray crystal structure of D5 in complex with 5-helix (PDB 2CMR) (59). (C) Schematic of D5 variants engineered and tested. The identity of each of the four CDR loops is represented by 0 (WT) or 1 (mutant).