Journal of Medicinal Chemistry · 2017 · 93 citations · 49 references
Life SciencesBiochemistryMolecular BiologyGene ExpressionMolecular Cell BiologyStructural BiologyChemical Probe DiscoveryMolecular Probe DevelopmentProtein DegradationProtein DesignProtein TargetingChemical Biology ProbesDrug-target EngagementPhysicochemical PropertiesProbe DesignProtein TargetsSmall Molecule TherapeuticsTargeted Molecular ProbesTargeted Protein Degradation
Demonstrating intracellular protein target engagement is an essential step in the development and progression of new chemical probes and potential small molecule therapeutics. However, this can be particularly challenging for poorly studied and noncatalytic proteins, as robust proximal biomarkers are rarely known. To confirm that our recently discovered chemical probe 1 (CCT251236) binds the putative transcription factor regulator pirin in living cells, we developed a heterobifunctional protein degradation probe. Focusing on linker design and physicochemical properties, we generated a highly active probe 16 (CCT367766) in only three iterations, validating our efficient strategy for degradation probe design against nonvalidated protein targets.
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