is currently the only small-molecule modulator in clinical trials targeting PD-L1 and VISTA proteins - important negative checkpoint regulators of immune activation. The reported therapeutic results to some extent mimic those of FDA-approved monoclonal antibodies overcoming the limitations of the high production costs and adverse effects of the latter. However, no conclusive biophysical evidence proving the binding to hPD-L1 has ever been presented. Using well-known in vitro methods: NMR binding assay, HTRF and cell-based activation assays, we clearly show that there is no direct binding between and PD-L1. To strengthen our reasoning, we performed control experiments on - a 29-mer peptide, which is a precursor of . Positive controls consisted of the well-documented small-molecule PD-L1 inhibitors: and .
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6695792 | PMC |
http://dx.doi.org/10.3390/molecules24152804 | DOI Listing |
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