NEMO recruitment at single cytokine-receptor complexes shows quantized dynamics independent of ligand affinity
Cells use a limited number of receptors to sense and process molecular information from their environment. In the classical view of signaling, receptor-ligand affinities determine binding kinetics, in timescales of diffusion, where their time-averaged contact duration regulates rapid cytoplasmic signaling events to coordinate cellular responses. For some cytokines, single receptor-ligand binding events can initiate large multiprotein complexes in the cytoplasm that assemble over tens of minutes, bringing to question how cytokine affinity influences the sensitivity and strength of signaling. Here, we leverage naturally occurring variation of IL-1{beta} from multiple species to determine the impact of affinity on human IL-1 receptor signaling. Using experiments and models we investigate single receptor complexes activated by ligands that vary across multiple orders of magnitude in affinity. Our results show that while the receptor-ligand affinity establishes cytokine response sensitivity, activated IL-1 receptor complexes signal as discrete, quantized packets of signaling flux independent of affinity.