Abstract
Inflammasomes are high molecular weight complexes that play an integral role in the innate immune system, triggering an inflammatory cascade to protect against cellular stresses such as pathogenic bacteria. Both canonical and non-canonical inflammasomes have been described in the literature and detailed structural studies of many components of the more complex and larger canonical versions have been reported. In contrast, corresponding structures of the non-canonical inflammasome have not emerged even though it consists of only two components: lipopolysaccharide (LPS) from gram-negative bacteria, and one of caspase-4 or caspase-5 in humans or caspase-11 in mice. Here we determine the stoichiometry of the non-canonical inflammasome using size-exclusion chromatography coupled with UV, refractive index, and light-scattering measurements, showing that the non-canonical inflammasome is heterogeneous, comprised of three major complexes with different numbers of LPS and caspase molecules. Solution Nuclear Magnetic Resonance (NMR) spectroscopy studies of the N-terminal Caspase Activation and Recruitment Domain (CARD) of caspase-11, that binds LPS, show that it is largely unstructured in the absence of lipid, with pervasive dynamics on the μs-ms timescale. Formation of this complex increases the alpha-helical content of the CARD but the dynamics persist, multiple conformers are formed, and tertiary contacts are transient, consistent with formation of a molten globule. Our NMR results establish that the protease domain of caspase-11 is monomeric in isolation. As proteolysis is linked with dimerization, the protease domains are inactive in this state, but upon formation of the non-canonical inflammasome dimerization occurs, priming the complex for rapid processing of substrates. SIGNIFICANCE STATEMENT: Animals respond to injury, infection, or toxic materials via a process called inflammation. At the molecular level inflammation involves formation of large machines - inflammasomes - that are instrumental in triggering cascades that lead to an immune response. Although structural studies of canonical inflammasomes have emerged, much less is known about the structures of non-canonical inflammasomes. Using solution Nuclear Magnetic Resonance (NMR) spectroscopy in concert with other biophysical approaches we show that non-canonical inflammasomes are highly dynamic and structurally heterogeneous, and we characterize the different sized inflammasome particles that are formed in terms of their composition. We also show that once formed, non-canonical inflammasomes are primed to rapidly cleave substrate molecules, necessary for propagating the immune response.