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Terphenyl-Based Small-Molecule Inhibitors of Programmed Cell Death-1/Programmed Death-Ligand 1 Protein–Protein Interaction

Damian Muszak, Ewa Surmiak, Jacek Plewka, Katarzyna Magiera‐Mularz, Justyna Kocik-Krol, Bogdan Musielak, Dominik Sala, Radosław Kitel, Małgorzata Stec, Kazimierz Węglarczyk, Maciej Siedlar, Alexander Dömlingꝉ, Łukasz Skalniak, Tad A. Holak

2021Journal of Medicinal Chemistry91 citationsDOIOpen Access PDF

Abstract

docking, we designed and then experimentally demonstrated the effectiveness of the terphenyl-based scaffolds in inhibiting PD-1/PD-L1 complex formation using various biophysical and biochemical techniques. We also present a high-resolution structure of the complex of PD-L1 with one of our most potent inhibitors to identify key PD-L1/inhibitor interactions at the molecular level. In addition, we show the efficacy of our most potent inhibitors in activating the antitumor response using primary human immune cells from healthy donors.

Topics & Concepts

ChemistryIn silicoTerphenylDocking (animal)Small moleculeProgrammed cell deathScaffoldLigand (biochemistry)Computational biologyStereochemistryBiochemistryApoptosisReceptorNursingMedicineGeneBiomedical engineeringOrganic chemistryBiologyCancer Immunotherapy and BiomarkersCAR-T cell therapy researchPharmacological Receptor Mechanisms and Effects
Terphenyl-Based Small-Molecule Inhibitors of Programmed Cell Death-1/Programmed Death-Ligand 1 Protein–Protein Interaction | Litcius