CA-170 - A Potent Small-Molecule PD-L1 Inhibitor or Not?
Bogdan M MusielakJustyna Kocik-KrolŁukasz SkalniakKatarzyna Magiera-MularzDominik SalaMiroslawa CzubMalgorzata StecMaciej SiedlarTad A HolakJacek PlewkaPublished in: Molecules (Basel, Switzerland) (2019)
CA-170 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 CA-170 and PD-L1. To strengthen our reasoning, we performed control experiments on AUNP-12 - a 29-mer peptide, which is a precursor of CA-170. Positive controls consisted of the well-documented small-molecule PD-L1 inhibitors: BMS-1166 and peptide-57.
Keyphrases
- small molecule
- protein protein
- clinical trial
- high throughput
- protein kinase
- dna damage
- magnetic resonance
- single cell
- transcription factor
- high resolution
- cell cycle
- dna binding
- stem cells
- binding protein
- mass spectrometry
- randomized controlled trial
- drug delivery
- electronic health record
- adverse drug
- human serum albumin