Design and validation of a synthetic VH repertoire with tailored diversity for protein recognition

Previous studies have indicated differences in the specificity‐determining residues (SDRs) of antibodies that recognize haptens, peptides, or proteins. Here, we designed a VH repertoire based on the human scaffold 3‐23/JH4 and diversification of high and medium‐usage SDRs of anti‐protein and anti‐peptide antibodies. The repertoire was synthesized by overlapping polymerase chain reaction (PCR) and combined with the VL chain of the anti‐hen egg‐white lysozyme (HEL) antibody D1.3. The resulting chimeric single‐chain Fv fragments (scFvs) phage‐displayed library was panned in HEL‐coated immunotubes. After two rounds of selection under non‐stringent conditions, that is, trypsinization after 2 h of incubation at room temperature, 63 of 167 clones analyzed (38%) were found to express scFvs specific to HEL. Twenty clones were characterized by DNA sequencing resulting in 10 unique scFvs. Interestingly, the panel of unique scFvs was highly diverse, with VH sequences differing in 16 of the 17 positions variegated in the repertoire. Thus, diverse chemico‐physical and structural solutions were selected from the library, even when the VH repertoire was constrained by the VL chain of D1.3 to yield binders against a definite region of HEL surface. The more often selected scFvs, namely H6‐1 and B7‐1, which differed in eight SDRs, showed levels of expression in E. coli TG1 strain, 6 and 10 times higher than the parental D1.3 Fv fragment, respectively. Dissociation constants (KDs) measured in the BIAcore were 11 and 6.6 nM for H6‐1 and B7‐1, respectively. These values compared well to the KD of 4.7 nM measured for D1.3, indicating that the VH repertoire here designed is a valuable source of diverse, well‐expressed and high affinity VH domains. Copyright © 2006 John Wiley & Sons, Ltd.