Deconstruction of Dual-Site Tankyrase Inhibitors Provides Insights into Binding Energetics and Suggests Critical Hotspots for Ligand Optimization

Designing inhibitors is a complex task that requires a deep understanding of protein-ligand interactions and their dynamics. Ligands often interact with multiple binding subsites, with noncovalent interactions affecting binding affinity. Conformational changes and plasticity of both, the ligand and the protein influence binding energetics. We investigated the tankyrase ADP-ribosyltransferase as a promising drug target regulating many cellular pathways. Despite the existence of diverse tankyrase inhibitors, their binding energetics and contributions of flexible cryptic subpockets to binding affinity remain elusive. To examine these aspects, we deconstructed inhibitors to key fragments, dissected their energetic contribution to the affinity, and determined their binding mode by X-ray crystallography. Varying ligand efficiencies of the deconstructed, pocket-binding fragments revealed the cryptic nature of subpockets. These insights enabled us to redesign inhibitors with novel linkers, the observed key area for optimization, increasing the potency in enzymatic and cell-based assays by 7.5-fold and 6.2-fold compared to the parent ligand.

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Publication Details

Journal
Journal of Medicinal Chemistry
Published
2025-03-26
DOI
https://doi.org/10.1021/acs.jmedchem.4c02845
Citations
1
Primary Topic
Wnt/β-catenin signaling in development and cancer
Type
article
Field-Weighted Citation Impact
0.81

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article

Deconstruction of Dual-Site Tankyrase Inhibitors Provides Insights into Binding Energetics and Suggests Critical Hotspots for Ligand Optimization

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1 citations
Journal of Medicinal Chemistry
Wnt/β-catenin signaling in development and cancer
0.81
article

Deconstruction of Dual-Site Tankyrase Inhibitors Provides Insights into Binding Energetics and Suggests Critical Hotspots for Ligand Optimization

Chiara Bosetti, Davide Cirillo, Stefan Johannes Karl Krauss, Ruben G.G. Leenders, Yelena Mostinski, Jo Waaler, Marc Nazaré, Andrea Volkamer, L. Lehtiö, Carolina S. Vinagreiro, Murat Kücükdisli, Sven T. Sowa, David Schaller, Anita Wegert, Shoshy Alam Brinch, Kirsten van Laar
article en
1 citations

Abstract

Designing inhibitors is a complex task that requires a deep understanding of protein-ligand interactions and their dynamics. Ligands often interact with multiple binding subsites, with noncovalent interactions affecting binding affinity. Conformational changes and plasticity of both, the ligand and the protein influence binding energetics. We investigated the tankyrase ADP-ribosyltransferase as a promising drug target regulating many cellular pathways. Despite the existence of diverse tankyrase inhibitors, their binding energetics and contributions of flexible cryptic subpockets to binding affinity remain elusive. To examine these aspects, we deconstructed inhibitors to key fragments, dissected their energetic contribution to the affinity, and determined their binding mode by X-ray crystallography. Varying ligand efficiencies of the deconstructed, pocket-binding fragments revealed the cryptic nature of subpockets. These insights enabled us to redesign inhibitors with novel linkers, the observed key area for optimization, increasing the potency in enzymatic and cell-based assays by 7.5-fold and 6.2-fold compared to the parent ligand.

Journal of Medicinal ChemistryVol. 68(7)
Oslo University Hospital (NO), University of Oslo (NO), Leibniz-Forschungsinstitut für Molekulare Pharmakologie (DE), Flevoziekenhuis (NL), Charité - Universitätsmedizin Berlin (DE), Saarland University (DE), University of Oulu (FI)
Minerva Foundation, Jane ja Aatos Erkon Säätiö, Helse Sør-Øst RHF
Openalex Percentile: Top 30%
Wnt/β-catenin signaling in development and cancer
0.81
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