Reversible Antagonism of Dopamine D1 Receptor Using a Photoswitchable Remotely Tethered Ligand

Dopamine D1 receptor (D1R) plays key roles in health and disease. D1R is broadly expressed throughout the brain and body and is dynamically activated in response to endogenous dopamine, making it difficult to target this receptor with sufficient precision. We previously developed a robust light-activatable, tetherable agonist for D1R, wherein a temporally precise photoswitch (the P compound) binds to a genetically encoded membrane anchoring protein (the M protein) in specific brain locations and cell types. Here we extended our approach by developing a complementary antagonist P compound that could be used to block specific populations of D1R in the brain with precise timing. Together, we have generated a robust toolkit for interrogating D1R function in the brain with unprecedented precision.

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Publication Details

Journal
ACS Chemical Biology
Published
2025-10-16
DOI
https://doi.org/10.1021/acschembio.5c00441
Primary Topic
Photochromic and Fluorescence Chemistry
Type
article
Field-Weighted Citation Impact
0.00
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article

Reversible Antagonism of Dopamine D1 Receptor Using a Photoswitchable Remotely Tethered Ligand

Prashant Donthamsetti, Dirk H. Trauner, Robert M. Wolesensky, Belinda E. Hetzler et al.
ACS Chemical Biology
Photochromic and Fluorescence Chemistry
article

Reversible Antagonism of Dopamine D1 Receptor Using a Photoswitchable Remotely Tethered Ligand

Prashant Donthamsetti, Dirk H. Trauner, Robert M. Wolesensky, Belinda E. Hetzler, Cherise Stanley, Ehud Y. Isacoff
article en

Abstract

Dopamine D1 receptor (D1R) plays key roles in health and disease. D1R is broadly expressed throughout the brain and body and is dynamically activated in response to endogenous dopamine, making it difficult to target this receptor with sufficient precision. We previously developed a robust light-activatable, tetherable agonist for D1R, wherein a temporally precise photoswitch (the P compound) binds to a genetically encoded membrane anchoring protein (the M protein) in specific brain locations and cell types. Here we extended our approach by developing a complementary antagonist P compound that could be used to block specific populations of D1R in the brain with precise timing. Together, we have generated a robust toolkit for interrogating D1R function in the brain with unprecedented precision.

ACS Chemical BiologyVol. 20(11)
Lawrence Berkeley National Laboratory (US), Vanderbilt University (US), University of California System (US), Institute of Molecular Bioimaging and Physiology (IT), Neuroscience Institute (IT), Institute of Molecular Biology and Biophysics (RU), New York University (US), University of California, Berkeley (US)
Openalex Percentile: Top 77%
Photochromic and Fluorescence Chemistry
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