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8P1O

Solubilizer tag effect on PD-L1/inhibitor binding properties for m-terphenyl derivatives

Summary for 8P1O
Entry DOI10.2210/pdb8p1o/pdb
DescriptorProgrammed cell death 1 ligand 1, (3~{R})-1-[[4-[2-chloranyl-3-(2,3-dihydro-1,4-benzodioxin-6-yl)phenyl]-2-methoxy-phenyl]methyl]-~{N}-(2-hydroxyethyl)pyrrolidine-3-carboxamide, CHLORIDE ION, ... (5 entities in total)
Functional Keywordspd-l1, immune checkpoint, small-molecule inhibitor, cancer, m-terphenyl, immune system
Biological sourceHomo sapiens (human)
Total number of polymer chains2
Total formula weight34254.56
Authors
Plewka, J.,Magiera-Mularz, K.,Surmiak, E.,Kalinowska-Tluscik, J.,Holak, T.A. (deposition date: 2023-05-12, release date: 2024-01-31, Last modification date: 2024-10-09)
Primary citationSurmiak, E.,Zaber, J.,Plewka, J.,Wojtanowicz, G.,Kocik-Krol, J.,Kruc, O.,Muszak, D.,Rodriguez, I.,Musielak, B.,Viviano, M.,Castellano, S.,Skalniak, L.,Magiera-Mularz, K.,Holak, T.A.,Kalinowska-Tluscik, J.
Solubilizer Tag Effect on PD-L1/Inhibitor Binding Properties for m -Terphenyl Derivatives.
Acs Med.Chem.Lett., 15:36-44, 2024
Cited by
PubMed Abstract: Although heavily studied, the subject of anti-PD-L1 small-molecule inhibitors is still elusive. Here we present a systematic overview of the principles behind successful anti-PD-L1 small-molecule inhibitor design on the example of the -terphenyl scaffold, with a particular focus on the neglected influence of the solubilizer tag on the overall affinity toward PD-L1. The inhibitor developed according to the proposed guidelines was characterized through its potency in blocking PD-1/PD-L1 complex formation in homogeneous time-resolved fluorescence and cell-based assays. The affinity is also explained based on the crystal structure of the inhibitor itself and its costructure with PD-L1 as well as a molecular modeling study. Our results structuralize the knowledge related to the strong pharmacophore feature of the -terphenyl scaffold preferential geometry and the more complex role of the solubilizer tag in PD-L1 homodimer stabilization.
PubMed: 38229762
DOI: 10.1021/acsmedchemlett.3c00306
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.17 Å)
Structure validation

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