P03 - Identification and functional characterization of the TRPP2 channel complex
Mutations in transient receptor potential channel polycystin-2 (TRPP2) cause autosomal dominant polycystic kidney disease (ADPKD). TRPP2 is a Ca2+-permeable non-selective cation channel, but it is not known how TRPP2 channel activity translates into morphogenetic programs. We hypothesize that local Ca2+ signals are critical to regulate specific downstream factors in TRPP2 signaling micro-domains. The molecular composition of the TRPP2 complex at the core of these micro-domains is unknown. Therefore, the goal of this proposal is to identify and characterize the proteins constituting the native TRPP2 complex in order to understand the role of TRPP2-mediated signaling in health and disease.