Epitope mapping reveals the binding mechanism of a functional antibody cross-reactive to both human and murine programmed death 1

D Li, J Xu, Z Wang, Z Gong, J Liu, Y Zheng, J Li, J Li - MAbs, 2017 - Taylor & Francis
D Li, J Xu, Z Wang, Z Gong, J Liu, Y Zheng, J Li, J Li
MAbs, 2017Taylor & Francis
Of the inhibitory checkpoints in the immune system, programmed death 1 (PD-1) is one of
the most promising targets for cancer immunotherapy. The anti-PD-1 antibodies currently
approved for clinical use or under development bind to human PD-1 (hPD-1), but not murine
PD-1. To facilitate studies in murine models, we developed a functional antibody against
both human and murine PD-1, and compared the epitopes of such antibody to a counterpart
that only bound to hPD-1. To quickly identify the epitopes of the 2 antibodies, we used …
Abstract
Of the inhibitory checkpoints in the immune system, programmed death 1 (PD-1) is one of the most promising targets for cancer immunotherapy. The anti-PD-1 antibodies currently approved for clinical use or under development bind to human PD-1 (hPD-1), but not murine PD-1. To facilitate studies in murine models, we developed a functional antibody against both human and murine PD-1, and compared the epitopes of such antibody to a counterpart that only bound to hPD-1. To quickly identify the epitopes of the 2 antibodies, we used alanine scanning and mammalian cell expression cassette. The epitope identification was based on PD-1-binding ELISA and supported by affinity ranking of surface plasmon resonance results. The hPD-1 epitopes of the 2 functional antibodies were also compared with the binding region on hPD-1 that is responsible for PD-L1 interaction. In silico modeling were conducted to explain the different binding modes of the 2 antibodies, suggesting a potential mechanism of the antibody cross-species binding.
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