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

MAbs. 2017 May/Jun;9(4):628-637. doi: 10.1080/19420862.2017.1296612. Epub 2017 Feb 23.

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.

Keywords: Cross-species binding; Programmed death 1 (PD-1); epitope mapping; functional antibody; modeling.

MeSH terms

  • Animals
  • Antibodies / chemistry*
  • Cross Reactions
  • Enzyme-Linked Immunosorbent Assay / methods
  • Epitope Mapping / methods*
  • Humans
  • Mice
  • Molecular Docking Simulation*
  • Programmed Cell Death 1 Receptor / chemistry*

Substances

  • Antibodies
  • PDCD1 protein, human
  • Pdcd1 protein, mouse
  • Programmed Cell Death 1 Receptor