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An Improved Ras Sensor for Highly Sensitive and Quantitative FRET-FLIM Imaging

Ras is a signaling protein involved in a variety of cellular processes. Hence, studying Ras signaling with high spatiotemporal resolution is crucial to understanding the roles of Ras in many important cellular functions. Previously, fluorescence lifetime imaging (FLIM) of fluorescent resonance energ...

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Detalles Bibliográficos
Autores principales: Oliveira, Ana F., Yasuda, Ryohei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3544822/
https://www.ncbi.nlm.nih.gov/pubmed/23349692
http://dx.doi.org/10.1371/journal.pone.0052874
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author Oliveira, Ana F.
Yasuda, Ryohei
author_facet Oliveira, Ana F.
Yasuda, Ryohei
author_sort Oliveira, Ana F.
collection PubMed
description Ras is a signaling protein involved in a variety of cellular processes. Hence, studying Ras signaling with high spatiotemporal resolution is crucial to understanding the roles of Ras in many important cellular functions. Previously, fluorescence lifetime imaging (FLIM) of fluorescent resonance energy transfer (FRET)-based Ras activity sensors, FRas and FRas-F, have been demonstrated to be useful for measuring the spatiotemporal dynamics of Ras signaling in subcellular micro-compartments. However the predominantly nuclear localization of the sensors' acceptor has limited its sensitivity. Here, we have overcome this limitation and developed two variants of the existing FRas sensor with different affinities: FRas2-F (K(d)∼1.7 µM) and FRas2-M (K(d)∼0.5 µM). We demonstrate that, under 2-photon fluorescence lifetime imaging microscopy, FRas2 sensors provide higher sensitivity compared to previous sensors in 293T cells and neurons.
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spelling pubmed-35448222013-01-24 An Improved Ras Sensor for Highly Sensitive and Quantitative FRET-FLIM Imaging Oliveira, Ana F. Yasuda, Ryohei PLoS One Research Article Ras is a signaling protein involved in a variety of cellular processes. Hence, studying Ras signaling with high spatiotemporal resolution is crucial to understanding the roles of Ras in many important cellular functions. Previously, fluorescence lifetime imaging (FLIM) of fluorescent resonance energy transfer (FRET)-based Ras activity sensors, FRas and FRas-F, have been demonstrated to be useful for measuring the spatiotemporal dynamics of Ras signaling in subcellular micro-compartments. However the predominantly nuclear localization of the sensors' acceptor has limited its sensitivity. Here, we have overcome this limitation and developed two variants of the existing FRas sensor with different affinities: FRas2-F (K(d)∼1.7 µM) and FRas2-M (K(d)∼0.5 µM). We demonstrate that, under 2-photon fluorescence lifetime imaging microscopy, FRas2 sensors provide higher sensitivity compared to previous sensors in 293T cells and neurons. Public Library of Science 2013-01-14 /pmc/articles/PMC3544822/ /pubmed/23349692 http://dx.doi.org/10.1371/journal.pone.0052874 Text en © 2013 Oliveira, Yasuda http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Oliveira, Ana F.
Yasuda, Ryohei
An Improved Ras Sensor for Highly Sensitive and Quantitative FRET-FLIM Imaging
title An Improved Ras Sensor for Highly Sensitive and Quantitative FRET-FLIM Imaging
title_full An Improved Ras Sensor for Highly Sensitive and Quantitative FRET-FLIM Imaging
title_fullStr An Improved Ras Sensor for Highly Sensitive and Quantitative FRET-FLIM Imaging
title_full_unstemmed An Improved Ras Sensor for Highly Sensitive and Quantitative FRET-FLIM Imaging
title_short An Improved Ras Sensor for Highly Sensitive and Quantitative FRET-FLIM Imaging
title_sort improved ras sensor for highly sensitive and quantitative fret-flim imaging
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3544822/
https://www.ncbi.nlm.nih.gov/pubmed/23349692
http://dx.doi.org/10.1371/journal.pone.0052874
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