Non fitting based FRET-FLIM analysis approaches applied to quantify protein-protein interactions in live cells

New imaging methodologies in quantitative fluorescence microscopy and nanoscopy have been developed in the last few years and are beginning to be extensively applied to biological problems, such as the localization and quantification of protein interactions. Fluorescence resonance energy transfer (F...

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Asıl Yazarlar: Padilla-Parra, S, Auduge, N, Coppey-Moisan, M, Tramier, M
Materyal Türü: Journal article
Dil:English
Baskı/Yayın Bilgisi: 2011
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author Padilla-Parra, S
Auduge, N
Coppey-Moisan, M
Tramier, M
author_facet Padilla-Parra, S
Auduge, N
Coppey-Moisan, M
Tramier, M
author_sort Padilla-Parra, S
collection OXFORD
description New imaging methodologies in quantitative fluorescence microscopy and nanoscopy have been developed in the last few years and are beginning to be extensively applied to biological problems, such as the localization and quantification of protein interactions. Fluorescence resonance energy transfer (FRET) detected by fluorescence lifetime imaging microscopy (FLIM) is currently employed not only in biophysics or chemistry but also in bio-medicine, thanks to new advancements in technology and also new developments in data treatment. FRET-FLIM can be a very useful tool to ascertain protein interactions occurring in single living cells. In this review, we stress the importance of increasing the acquisition speed when working in vivo employing Time-Domain FLIM. The development of the new mathematical-based non-fitting methods allows the determining of the fraction of interacting donor without the requirement of high count statistics, and thus allows the performing of high speed acquisitions in FRET-FLIM to still be quantitative. © 2011 International Union for Pure and Applied Biophysics (IUPAB) and Springer.
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spelling oxford-uuid:29fbd294-8f64-412a-8772-a4bd0d602b2b2022-03-26T12:22:12ZNon fitting based FRET-FLIM analysis approaches applied to quantify protein-protein interactions in live cellsJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:29fbd294-8f64-412a-8772-a4bd0d602b2bEnglishSymplectic Elements at Oxford2011Padilla-Parra, SAuduge, NCoppey-Moisan, MTramier, MNew imaging methodologies in quantitative fluorescence microscopy and nanoscopy have been developed in the last few years and are beginning to be extensively applied to biological problems, such as the localization and quantification of protein interactions. Fluorescence resonance energy transfer (FRET) detected by fluorescence lifetime imaging microscopy (FLIM) is currently employed not only in biophysics or chemistry but also in bio-medicine, thanks to new advancements in technology and also new developments in data treatment. FRET-FLIM can be a very useful tool to ascertain protein interactions occurring in single living cells. In this review, we stress the importance of increasing the acquisition speed when working in vivo employing Time-Domain FLIM. The development of the new mathematical-based non-fitting methods allows the determining of the fraction of interacting donor without the requirement of high count statistics, and thus allows the performing of high speed acquisitions in FRET-FLIM to still be quantitative. © 2011 International Union for Pure and Applied Biophysics (IUPAB) and Springer.
spellingShingle Padilla-Parra, S
Auduge, N
Coppey-Moisan, M
Tramier, M
Non fitting based FRET-FLIM analysis approaches applied to quantify protein-protein interactions in live cells
title Non fitting based FRET-FLIM analysis approaches applied to quantify protein-protein interactions in live cells
title_full Non fitting based FRET-FLIM analysis approaches applied to quantify protein-protein interactions in live cells
title_fullStr Non fitting based FRET-FLIM analysis approaches applied to quantify protein-protein interactions in live cells
title_full_unstemmed Non fitting based FRET-FLIM analysis approaches applied to quantify protein-protein interactions in live cells
title_short Non fitting based FRET-FLIM analysis approaches applied to quantify protein-protein interactions in live cells
title_sort non fitting based fret flim analysis approaches applied to quantify protein protein interactions in live cells
work_keys_str_mv AT padillaparras nonfittingbasedfretflimanalysisapproachesappliedtoquantifyproteinproteininteractionsinlivecells
AT audugen nonfittingbasedfretflimanalysisapproachesappliedtoquantifyproteinproteininteractionsinlivecells
AT coppeymoisanm nonfittingbasedfretflimanalysisapproachesappliedtoquantifyproteinproteininteractionsinlivecells
AT tramierm nonfittingbasedfretflimanalysisapproachesappliedtoquantifyproteinproteininteractionsinlivecells