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J Med Chem ; 66(7): 4827-4839, 2023 04 13.
Artigo em Inglês | MEDLINE | ID: mdl-36994595

RESUMO

Covalent ligands are generally filtered out of chemical libraries used for high-throughput screening, because electrophilic functional groups are considered to be pan-assay interference compounds (PAINS). Therefore, screening strategies that can distinguish true covalent ligands from PAINS are required. Hydrogen/deuterium-exchange mass spectrometry (HDX-MS) is a powerful tool for evaluating protein stability. Here, we report a covalent modifier screening approach using HDX-MS. In this study, HDX-MS was used to classify peroxisome proliferator-activated receptor γ (PPARγ) and vitamin D receptor ligands. HDX-MS could discriminate the strength of ligand-protein interactions. Our HDX-MS screening method identified LT175 and nTZDpa, which can bind concurrently to the PPARγ ligand-binding domain (PPARγ-LBD) with synergistic activation. Furthermore, iodoacetic acid was identified as a novel covalent modifier that stabilizes the PPARγ-LBD.


Assuntos
Espectrometria de Massa com Troca Hidrogênio-Deutério , PPAR gama , Deutério/química , Ligantes , PPAR gama/química , Espectrometria de Massas/métodos , Medição da Troca de Deutério/métodos
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