Cell specific photoswitchable agonist for reversible control of endogenous dopamine receptors

Donthamsetti, Prashant; Winter, Nils; Hoagland, Adam; Stanley, Cherise; Visel, Meike; Lammel, Stephan; Trauner, Dirk; Isacoff, Ehud

doi:10.1038/s41467-021-25003-w

Title: Cell specific photoswitchable agonist for reversible control of endogenous dopamine receptors

Journal Article · Fri Aug 06 00:00:00 UTC 2021 · Nature Communications

DOI: https://doi.org/10.1038/s41467-021-25003-w · OSTI ID:2470970

Donthamsetti, Prashant ^[1]; Winter, Nils ^[2]; Hoagland, Adam ^[1]; Stanley, Cherise ^[1]; Visel, Meike ^[1];

^[1];

^[3];

^[4]

University of California, Berkeley, CA (United States)
Ludwig-Maximilians University, München (Germany)
New York University, NY (United States)
University of California, Berkeley, CA (United States); Lawrence Berkeley National Laboratory (LBNL), Berkeley, CA (United States)

Dopamine controls diverse behaviors and their dysregulation contributes to many disorders. Our ability to understand and manipulate the function of dopamine is limited by the heterogenous nature of dopaminergic projections, the diversity of neurons that are regulated by dopamine, the varying distribution of the five dopamine receptors (DARs), and the complex dynamics of dopamine release. In order to improve our ability to specifically modulate distinct DARs, here we develop a photo-pharmacological strategy using a Membrane anchored Photoswitchable orthogonal remotely tethered agonist for the Dopamine receptor (MP-D). Our design selectively targets D1R/D5R receptor subtypes, most potently D1R (MP-D1_ago), as shown in HEK293T cells. In vivo, we targeted dorsal striatal medium spiny neurons where the photo-activation of MP-D1_ago increased movement initiation, although further work is required to assess the effects of MP-D1_ago on neuronal function. Our method combines ligand and cell type-specificity with temporally precise and reversible activation of D1R to control specific aspects of movement. Our results provide a template for analyzing dopamine receptors.

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Research Organization:: Lawrence Berkeley National Laboratory (LBNL), Berkeley, CA (United States)

Sponsoring Organization:: USDOE

Grant/Contract Number:: AC02-05CH11231

OSTI ID:: 2470970

Journal Information:: Nature Communications, Journal Name: Nature Communications Journal Issue: 1 Vol. 12; ISSN 2041-1723

Publisher:: Nature Publishing GroupCopyright Statement

Country of Publication:: United States

Language:: English

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