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.

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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
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article

Aryl azopyrroles as visible light photoswitchable TRPA1 ligands

Philip J. Parsons, Peter Haycock, Matthew J. Fuchter, Kai Zheng et al.
1 citations
Chemical Science
Photochromic and Fluorescence Chemistry
0.52
article

Aryl azopyrroles as visible light photoswitchable TRPA1 ligands

Philip J. Parsons, Peter Haycock, Matthew J. Fuchter, Kai Zheng, Randall T. Peterson, Pui‐Ying Lam, Rui Tao, Lisa Carina Dollhopf, Jordan A Munos
article en
1 citations

Abstract

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.

Chemical ScienceVol. 16(42)
Mansfield University (US), Medical College of Wisconsin (US), University of Utah (US), Oxford Research Group (GB), University of Oxford (GB), Imperial College London (GB)
Openalex Percentile: Top 33%
Photochromic and Fluorescence Chemistry
0.52
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Aryl azopyrroles as visible light photoswitchable TRPA1 ligands — Philip J. Parsons, Peter Haycock, et al. · Chemical Science (2025) | TGRS Research Map | TGRS