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Unraveling the hidden temporal range of fast β(2)-adrenergic receptor mobility by time-resolved fluorescence
G-protein-coupled receptors (GPCRs) are hypothesized to possess molecular mobility over a wide temporal range. Until now the temporal range has not been fully accessible due to the crucially limited temporal range of available methods. This in turn, may lead relevant dynamic constants to remain mask...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8885909/ https://www.ncbi.nlm.nih.gov/pubmed/35228644 http://dx.doi.org/10.1038/s42003-022-03106-4 |
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author | Balakrishnan, Ashwin Hemmen, Katherina Choudhury, Susobhan Krohn, Jan-Hagen Jansen, Kerstin Friedrich, Mike Beliu, Gerti Sauer, Markus Lohse, Martin J. Heinze, Katrin G. |
author_facet | Balakrishnan, Ashwin Hemmen, Katherina Choudhury, Susobhan Krohn, Jan-Hagen Jansen, Kerstin Friedrich, Mike Beliu, Gerti Sauer, Markus Lohse, Martin J. Heinze, Katrin G. |
author_sort | Balakrishnan, Ashwin |
collection | PubMed |
description | G-protein-coupled receptors (GPCRs) are hypothesized to possess molecular mobility over a wide temporal range. Until now the temporal range has not been fully accessible due to the crucially limited temporal range of available methods. This in turn, may lead relevant dynamic constants to remain masked. Here, we expand this dynamic range by combining fluorescent techniques using a spot confocal setup. We decipher mobility constants of β(2)-adrenergic receptor over a wide time range (nanosecond to second). Particularly, a translational mobility (10 µm²/s), one order of magnitude faster than membrane associated lateral mobility that explains membrane protein turnover and suggests a wider picture of the GPCR availability on the plasma membrane. And a so far elusive rotational mobility (1-200 µs) which depicts a previously overlooked dynamic component that, despite all complexity, behaves largely as predicted by the Saffman-Delbrück model. |
format | Online Article Text |
id | pubmed-8885909 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-88859092022-03-17 Unraveling the hidden temporal range of fast β(2)-adrenergic receptor mobility by time-resolved fluorescence Balakrishnan, Ashwin Hemmen, Katherina Choudhury, Susobhan Krohn, Jan-Hagen Jansen, Kerstin Friedrich, Mike Beliu, Gerti Sauer, Markus Lohse, Martin J. Heinze, Katrin G. Commun Biol Article G-protein-coupled receptors (GPCRs) are hypothesized to possess molecular mobility over a wide temporal range. Until now the temporal range has not been fully accessible due to the crucially limited temporal range of available methods. This in turn, may lead relevant dynamic constants to remain masked. Here, we expand this dynamic range by combining fluorescent techniques using a spot confocal setup. We decipher mobility constants of β(2)-adrenergic receptor over a wide time range (nanosecond to second). Particularly, a translational mobility (10 µm²/s), one order of magnitude faster than membrane associated lateral mobility that explains membrane protein turnover and suggests a wider picture of the GPCR availability on the plasma membrane. And a so far elusive rotational mobility (1-200 µs) which depicts a previously overlooked dynamic component that, despite all complexity, behaves largely as predicted by the Saffman-Delbrück model. Nature Publishing Group UK 2022-02-28 /pmc/articles/PMC8885909/ /pubmed/35228644 http://dx.doi.org/10.1038/s42003-022-03106-4 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Balakrishnan, Ashwin Hemmen, Katherina Choudhury, Susobhan Krohn, Jan-Hagen Jansen, Kerstin Friedrich, Mike Beliu, Gerti Sauer, Markus Lohse, Martin J. Heinze, Katrin G. Unraveling the hidden temporal range of fast β(2)-adrenergic receptor mobility by time-resolved fluorescence |
title | Unraveling the hidden temporal range of fast β(2)-adrenergic receptor mobility by time-resolved fluorescence |
title_full | Unraveling the hidden temporal range of fast β(2)-adrenergic receptor mobility by time-resolved fluorescence |
title_fullStr | Unraveling the hidden temporal range of fast β(2)-adrenergic receptor mobility by time-resolved fluorescence |
title_full_unstemmed | Unraveling the hidden temporal range of fast β(2)-adrenergic receptor mobility by time-resolved fluorescence |
title_short | Unraveling the hidden temporal range of fast β(2)-adrenergic receptor mobility by time-resolved fluorescence |
title_sort | unraveling the hidden temporal range of fast β(2)-adrenergic receptor mobility by time-resolved fluorescence |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8885909/ https://www.ncbi.nlm.nih.gov/pubmed/35228644 http://dx.doi.org/10.1038/s42003-022-03106-4 |
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