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Grga, J.

Publications and source records attributed to Grga, J..

3 recordsLinked to original sources

NLRP3 acts as a direct sensor of intracellular potassium ions

The NLRP3 inflammasome is a sentinel of cellular homeostasis, and its activation triggers the assembly of a molecular machinery that drives inflammation in infection, cardiovascular, metabolic, and neurodegenerative diseases. The majority of the many triggers known to activate NLRP3 are believed to induce potassium ion (K+) efflux from the cell as a fundamental danger signal for compromised cellular integrity. However, it has remained unclear how a reduction in intracellular K+ concentration is mechanistically translated into conformational changes in NLRP3 that promote inflammasome assembly, interleukin (IL)-1 release, and cell death. Here, we provide evidence that alterations in K+ levels directly regulate the conformation of the NLRP3 protein. In cell-free lysates derived from cell lines and primary blood immune cells high K+ concentrations stabilized a compact, protease-resistant structure resembling inhibitor-bound NLRP3, whereas low K+ conditions or the presence of a K+ chelator favored an open, more flexible and protease-accessible conformation. Notably, human NLRP3 remained responsive to K+ even when exogenously expressed in macrophage-like Drosophila cells or purified as recombinant protein. This indicates that K+ sensing occurs independently of cellular co-factors and is consistent with direct ion coordination. Of note, stimulation with the K+-independent NLRP3 agonist CL097 failed to recapitulate the conformational transition caused by K+ efflux inducer, nigericin. Moreover, pathogenic gain-of-function mutant variants of NLRP3 constitutively resembled the open and flexible protease-accessible conformation. Mapping K+-interactions by high-performance computation suggested that K+ ions populate the nucleotide binding pocket of the FISNA-NACHT module of individual NLRP3 chains but also stabilize face-to-face interactions within inactive oligomeric cage assemblies via the NACHT-adjacent acidic loop. Collectively, our findings enable us to propose a mechanistic model of how intracellular K+ ions preclude NLRP3 activation prior to efflux and thus how NLRP3 responds to cellular danger as a direct K+ sensing protein.

immunology↗

NMR at operational temperature for resonance assignments of a PET degrading enzyme

PETases are enzymes that can break down the poly-ethylene terephthalate (PET) polymer in its constituent building blocks. This enzymatic recycling process offers a sustainable solution for producing new, high-quality plastics from previously used materials. NMR spectroscopy can help in understanding and ultimately improving these enzymes but is always confronted with the lengthy step of acquisition and interpretation of triple resonance spectra for the spectral assignment. Here, we explore whether this step can be made more efficient by recording the spectra directly at high temperature, which simultaneously corresponds to more realistic working conditions for the enzyme. Taking the inactive variant of LCCICCG as an example, we compare spectral quality at 30{degrees}C and 50{degrees}C, and find that the latter condition greatly improves the Signal-to-Noise (S/N) ratio of the standard triple resonance spectra. Going up to 60{o}C, we show that pulse sequences mainly used for the assignment of intrinsically disordered proteins (IDPs) also become feasible. As a result, we present a methodology enabling exhaustive backbone assignment based on a minimal set of triple resonance spectra acquired and analysed in less than two weeks. The assignment process hence can be completed on a time scale comparable to crystallography, bringing NMR in a favourable position to contribute to bio-structural studies on this family of highly thermostable PETases.

biophysics↗

Non-decameric NLRP3 forms an MTOC-independent inflammasome

NLRP3 is an inflammasome-forming protein that plays a key role in conditions ranging from infections to Alzheimers disease. NLRP3 is activated by many potassium (K+)-dependent or - independent stimuli related to pathogens or sterile insults. Molecularly, human NLRP3 assembles into a decameric cage and its interaction with both the trans-Golgi network (TGN) and the microtubule organization centre (MTOC) has been proposed as critical for NLRP3 activation. However, the relative mechanistic requirement for K+-dependent versus - independent stimuli is unclear. Using spatially and dynamically high-resolution microscopy in human macrophages, we found that K+-dependent NLRP3 stimulation triggers two distinct activation pathways: (i) the decameric cage-dependent pathway, which was also exclusively required for the K+-independent stimulus, imiquimod; and (ii) a cage- and TGN/MTOC-independent pathway that was fully functional in an NLRP3 protein engineered to form monomers and unable to interact with membrane lipids. Collectively, our results delineate two parallel yet biologically distinct NLRP3 activation pathways.

molecular biology↗