Therapeutic targeting of the NLRP3 inflammasome, a pro-inflammatory macromolecular protein complex, has progressed beyond its early stages, with numerous compounds currently undergoing clinical evaluation. However, there remains a lack of clinically relevant biomarkers for assessing target engagement and efficacy of inflammasome inhibitors. While downstream inflammatory markers such as IL-6 and hsCRP are routinely assessed, their ability to accurately reflect the diverse aspects of inflammasome biology and serve as reliable biomarkers remains unclear.
This talk introduces PROTEINA’s Single-molecule Protein Interaction Detection (SPID) platform, which quantifies protein complexes at single-molecule resolution. By leveraging imaging data generated by the SPID platform, macromolecular protein complexes, such as inflammasomes, can be distinguished from monomeric proteins. Attendees will gain an understanding of how PROTEINA’s PPI PathFinder® assays work to directly quantify NLRP3 inflammasome assembly and activity, and how these assays can be applied to translational and clinical studies.
Key Topics:
- Beyond IL-6 and hsCRP: Direct quantification of NLRP3 inflammasome protein complex
- Assays on Focus: ASC speck and NLRP3-ASC complex
- Assays for Inflammasome Activity: Mature IL-1β and cleaved GSDMD
- Application to matrices: PBMC, serum, plasma and CSF
- Streamline translational studies: From mouse model assessment to GCLP analysis service for clinical trials