How to Make Bispecific Antibodies

Abstract

This protocol describes the production of bispecific F(ab’)2 antibody derivatives (BsAbs) by the linking of two Fab’ fragments via their hinge region SH groups using the bifunctional crosslinker o-phenylenedimaleimide (o-PDM) as described by Glennie et al. (1,2). The procedure is illustrated in Fig. 1. The first step is to obtain F(ab’)2 from the two parent IgG antibodies. Methods for digestion of IgG to F(ab’)2 are described in Chapter 25. Fab’ fragments are then prepared from the two F(ab’)₂ species by reduction with thiol, thus exposing free SH groups at the hinge region (three SH-groups for mouse IgG1 and IgG2a antibodies) (seeNote 1). One of the Fab’ species (Fab’-A) is selected for alkylation with o-PDM. Because o-PDM has a strong tendency to crosslink adjacent intramolecular SH-groups, two of the three hinge SH-groups will probably be linked together, leaving a single reactive maleimide group available for conjugation (Fig. 1; seeNote 2). Excess o-PDM is then removed by column chromatography, and the Fab’-A(mal) is mixed with the second reduced Fab’ (Fab’-B) under conditions favoring the crosslinking of the maleimide and SH groups. When equal amounts of the two parent Fab’ species are used, the major product is bispecific F(ab’)₂, resulting from the reaction of one Fab’-A(mal) with one of the SH groups at the hinge of Fab’-B. Increasing the proportion of Fab’-A(mal) in the reaction mixture results in a significant amount of F(ab’)₃ product by the reaction of two molecules of Fab’-A(mal) with two free SH-groups at the hinge of a single Fab’-B molecule (seeNote 3). The remaining free SH groups on Fab’-B are alkylated, and the F(ab’)₂ bispecific antibody product (Fab’-A x Fab’-B) is separated by gel filtration chromatography. Each stage of the procedure is checked by HPLC.