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Bispecific antibodies with Fab-arms featuring exchanged antigen-binding constant domains.


ABSTRACT: Monoclonal antibodies can acquire the property of engagement of a second antigen via fusion methods or modification of their CDR loops, but also by modification of their constant domains, such as in the mAb2 format where a set of mutated amino acid residues in the CH3 domains enables a high-affinity specific interaction with the second antigen. We tested the possibility of introducing multiple binding sites for the second antigen by replacing the Fab CH1/CL domain pair with a pair of antigen-binding CH3 domains in a model scaffold with trastuzumab variable domains and VEGF-binding CH3 domains. Such bispecific molecules were produced in a "Fab-like" format and in a full-length antibody format. Novel constructs were of expecte

SUBMITTER: Benedetti F 

PROVIDER: S-EPMC7920882 | biostudies-literature | 2021 Jul

REPOSITORIES: biostudies-literature