| Literature DB >> 28300475 |
Dong Li1, Jianqing Xu1, Zhuozhi Wang1, Zhen Gong2, Jieying Liu1, Yong Zheng1, Jian Li2, Jing Li1.
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.Entities:
Keywords: Cross-species binding; Programmed death 1 (PD-1); epitope mapping; functional antibody; modeling
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Year: 2017 PMID: 28300475 PMCID: PMC5419084 DOI: 10.1080/19420862.2017.1296612
Source DB: PubMed Journal: MAbs ISSN: 1942-0862 Impact factor: 5.857