A Small-Molecule Inhibitor to the Cytokine Interleukin-4.
Sean P QuinnellBecky S LeiferStephen T NestorKelly TanDaniel F SheehyLuke CeoShelby K DoyleAngela N KoehlerArturo J VegasPublished in: ACS chemical biology (2020)
Interleukin-4 (IL-4) is a multifunctional cytokine and an important regulator of inflammation. When deregulated, IL-4 activity is associated with asthma, allergic inflammation, and multiple types of cancer. While antibody-based inhibitors targeting the soluble cytokine have been evaluated clinically, they failed to achieve their end points in trials. Small-molecule inhibitors are an attractive alternative, but identifying effective chemotypes that inhibit the protein-protein interactions between cytokines and their receptors remains an active area of research. As a result, no small-molecule inhibitors to the soluble IL-4 cytokine have yet been reported. Here, we describe the first IL-4 small-molecule inhibitor identified and characterized through a combination of binding-based approaches and cell-based activity assays. The compound features a nicotinonitrile scaffold with micromolar affinity and potency for the cytokine and disrupts type II IL-4 signaling in cells. Small-molecule inhibitors of these important cell-signaling proteins have implications for numerous immune-related disorders and inform future drug discovery and design efforts for these challenging protein targets.
Keyphrases
- small molecule
- protein protein
- drug discovery
- oxidative stress
- single cell
- cell therapy
- induced apoptosis
- stem cells
- chronic obstructive pulmonary disease
- squamous cell carcinoma
- papillary thyroid
- transcription factor
- cell proliferation
- allergic rhinitis
- squamous cell
- lung function
- cell cycle arrest
- signaling pathway
- capillary electrophoresis
- atopic dermatitis
- childhood cancer