Aryl azopyrroles as visible light photoswitchable TRPA1 ligands
Access to high quality optochemogenetic tools will enable precise interrogation of the complex biology of diverse cell types, allowing temporally and spatially controlled manipulation of cell autonomous functions. This level of control is expected to yield deeper mechanistic insights and foster the development of targeted strategies and molecular interventions for translational photopharmacology. Recent years have demonstrated the exciting potential of heteroaromatic azoarene photoswitches, particularly to tune azo photoswitch performance. However, strategies to integrate such motifs into photopharmacological ligands remain underdeveloped. Leveraging a previously developed screening assay, we report the discovery of a robust aryl azopyrrole ligand for the TRPA1 channel, TRPswitch-C. TRPswitch-C provides a red-shifted chemotype to address this channel, allowing optical control in live zebrafish larvae in a controllable fashion. Not only does this study expand the tool kit for optochemogenetic experiments using TRPA1, but also advocates the further exploration of heteroaromatic azoarenes in photopharmacology.
Authors
- Philip J. Parsons (ORCID: https://orcid.org/0000-0002-9158-4034)
- Peter Haycock
- Matthew J. Fuchter (ORCID: https://orcid.org/0000-0002-1767-7072)
- Kai Zheng (ORCID: https://orcid.org/0000-0001-9275-1239)
- Randall T. Peterson (ORCID: https://orcid.org/0000-0003-0727-3469)
- Pui‐Ying Lam (ORCID: https://orcid.org/0000-0002-6319-5752)
- Rui Tao (ORCID: https://orcid.org/0000-0001-5234-6765)
- Lisa Carina Dollhopf
- Jordan A Munos
Institutions
- Mansfield University (US)
- Medical College of Wisconsin (US)
- University of Utah (US)
- Oxford Research Group (GB)
- University of Oxford (GB)
- Imperial College London (GB)
Publication Details
- Journal
- Chemical Science
- Published
- 2025-01-01
- DOI
- https://doi.org/10.1039/d5sc05070g
- Citations
- 1
- Primary Topic
- Photochromic and Fluorescence Chemistry
- Type
- article
- Field-Weighted Citation Impact
- 0.52