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  High-affinity functional fluorescent ligands for human β-adrenoceptors.

Mitronova, G., Lukinavicius, G., Butkevich, A., Kohl, T., Belov, V. N., Lehnart, S. E., et al. (2017). High-affinity functional fluorescent ligands for human β-adrenoceptors. Scientific Reports, 7: 12319. doi:10.1038/s41598-017-12468-3.

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Item Permalink: http://hdl.handle.net/11858/00-001M-0000-002D-FCD1-7 Version Permalink: http://hdl.handle.net/21.11116/0000-0001-A4E1-7
Genre: Journal Article

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 Creators:
Mitronova, G.1, Author              
Lukinavicius, G.2, Author              
Butkevich, A.1, Author              
Kohl, T., Author
Belov, V. N.1, Author              
Lehnart, S. E., Author
Hell, S. W.1, Author              
Affiliations:
1Department of NanoBiophotonics, MPI for Biophysical Chemistry, Max Planck Society, ou_578627              
2Laboratory of Chromatin Labeling and Imaging, Max Planck Institute for Biophysical Chemistry, Max Planck Society, ou_2616691              

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 Abstract: Visualization of the G-protein coupled receptor (GPCR) is of great importance for studying its function in a native cell. We have synthesized a series of red-emitting fluorescent probes targeting β-adrenergic receptor (βAR) that are compatible with confocal and Stimulated Emission Depletion (STED) microscopy as well as with Time-Resolved Fluorescence Resonance Energy Transfer (TR-FRET) binding assay in living cells. The probe based on the agonist BI-167107 and fluorescent dye KK114 demonstrates nanomolar binding affinity and up to nine-fold β2AR selectivity over β1AR. Carazolol-derived probes are fluorogenic and allow no-wash imaging experiments. STED microscopy of β2ARs stained at the native expression level on pancreatic CAPAN cells provides two-fold improvement in lateral optical resolution over confocal mode and reveals the formation of receptor microdomains. These probes retain their functional (agonist or antagonist) properties, allowing simultaneous modulation of cyclic adenosine monophosphate (cAMP) levels and receptor internalization as well as imaging receptor localization.

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Language(s): eng - English
 Dates: 2017-09-26
 Publication Status: Published online
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 Rev. Method: Peer
 Identifiers: DOI: 10.1038/s41598-017-12468-3
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Title: Scientific Reports
Source Genre: Journal
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Pages: 15 Volume / Issue: 7 Sequence Number: 12319 Start / End Page: - Identifier: -