Imaging of fluorescence anisotropy during photoswitching provides a simple readout for protein self-association
Performing homo-FRET measurements in cells using a fluorescence microscope is challenging, especially when using high numerical aperture objective lenses. Here the authors present a method for improved homo-FRET measurements based on anisotropy changes in photoswitchable fluorescent proteins.
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Nature Portfolio
2020
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oai:doaj.org-article:ab8c2a37ae65414495a695820bb8c70b2021-12-02T15:37:16ZImaging of fluorescence anisotropy during photoswitching provides a simple readout for protein self-association10.1038/s41467-019-13843-62041-1723https://doaj.org/article/ab8c2a37ae65414495a695820bb8c70b2020-01-01T00:00:00Zhttps://doi.org/10.1038/s41467-019-13843-6https://doaj.org/toc/2041-1723Performing homo-FRET measurements in cells using a fluorescence microscope is challenging, especially when using high numerical aperture objective lenses. Here the authors present a method for improved homo-FRET measurements based on anisotropy changes in photoswitchable fluorescent proteins.Namrata OjhaKristin H. RaineyGeorge H. PattersonNature PortfolioarticleScienceQENNature Communications, Vol 11, Iss 1, Pp 1-11 (2020) |
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Science Q |
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Science Q Namrata Ojha Kristin H. Rainey George H. Patterson Imaging of fluorescence anisotropy during photoswitching provides a simple readout for protein self-association |
description |
Performing homo-FRET measurements in cells using a fluorescence microscope is challenging, especially when using high numerical aperture objective lenses. Here the authors present a method for improved homo-FRET measurements based on anisotropy changes in photoswitchable fluorescent proteins. |
format |
article |
author |
Namrata Ojha Kristin H. Rainey George H. Patterson |
author_facet |
Namrata Ojha Kristin H. Rainey George H. Patterson |
author_sort |
Namrata Ojha |
title |
Imaging of fluorescence anisotropy during photoswitching provides a simple readout for protein self-association |
title_short |
Imaging of fluorescence anisotropy during photoswitching provides a simple readout for protein self-association |
title_full |
Imaging of fluorescence anisotropy during photoswitching provides a simple readout for protein self-association |
title_fullStr |
Imaging of fluorescence anisotropy during photoswitching provides a simple readout for protein self-association |
title_full_unstemmed |
Imaging of fluorescence anisotropy during photoswitching provides a simple readout for protein self-association |
title_sort |
imaging of fluorescence anisotropy during photoswitching provides a simple readout for protein self-association |
publisher |
Nature Portfolio |
publishDate |
2020 |
url |
https://doaj.org/article/ab8c2a37ae65414495a695820bb8c70b |
work_keys_str_mv |
AT namrataojha imagingoffluorescenceanisotropyduringphotoswitchingprovidesasimplereadoutforproteinselfassociation AT kristinhrainey imagingoffluorescenceanisotropyduringphotoswitchingprovidesasimplereadoutforproteinselfassociation AT georgehpatterson imagingoffluorescenceanisotropyduringphotoswitchingprovidesasimplereadoutforproteinselfassociation |
_version_ |
1718386251013292032 |