Probing PAC1 receptor activation across species with an engineered sensor

Elife. 2024 Aug 15:13:RP96496. doi: 10.7554/eLife.96496.

Abstract

Class-B1 G-protein-coupled receptors (GPCRs) are an important family of clinically relevant drug targets that remain difficult to investigate via high-throughput screening and in animal models. Here, we engineered PAClight1P78A, a novel genetically encoded sensor based on a class-B1 GPCR (the human PAC1 receptor, hmPAC1R) endowed with high dynamic range (ΔF/F0 = 1100%), excellent ligand selectivity, and rapid activation kinetics (τON = 1.15 s). To showcase the utility of this tool for in vitro applications, we thoroughly characterized and compared its expression, brightness and performance between PAClight1P78A-transfected and stably expressing cells. Demonstrating its use in animal models, we show robust expression and fluorescence responses upon exogenous ligand application ex vivo and in vivo in mice, as well as in living zebrafish larvae. Thus, the new GPCR-based sensor can be used for a wide range of applications across the life sciences empowering both basic research and drug development efforts.

Keywords: PAC1 receptor; PACAP; VIP; adenylate cyclase-activating polypeptide; biochemistry; chemical biology; genetically-encoded fluorescent sensors; human; mouse; neuropeptides; vasoactive intestinal peptide; zebrafish.

MeSH terms

  • Animals
  • Biosensing Techniques / methods
  • HEK293 Cells
  • Humans
  • Ligands
  • Mice
  • Protein Engineering / methods
  • Receptors, Pituitary Adenylate Cyclase-Activating Polypeptide, Type I / genetics
  • Receptors, Pituitary Adenylate Cyclase-Activating Polypeptide, Type I / metabolism
  • Zebrafish* / genetics
  • Zebrafish* / metabolism

Substances

  • Receptors, Pituitary Adenylate Cyclase-Activating Polypeptide, Type I
  • Ligands