Literature DB >> 22352644

Quantifying the influence of yellow fluorescent protein photoconversion on acceptor photobleaching-based fluorescence resonance energy transfer measurements.

Arne Seitz1, Stefan Terjung, Timo Zimmermann, Rainer Pepperkok.   

Abstract

Fluorescence resonance energy transfer (FRET) efficiency measurements based on acceptor photobleaching of yellow fluorescent protein (YFP) are affected by the fact that bleaching of YFP produces a fluorescent species that is detectable in cyan fluorescent protein (CFP) image channels. The presented quantitative measurement of this conversion makes it possible to correct the obtained FRET signal to increase the accuracy of intensity based CFP/YFP FRET measurements. The described method can additionally be used to compare samples with very different fluorescence levels.

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Year:  2012        PMID: 22352644     DOI: 10.1117/1.JBO.17.1.011010

Source DB:  PubMed          Journal:  J Biomed Opt        ISSN: 1083-3668            Impact factor:   3.170


  3 in total

1.  Optimizing fluorescent protein trios for 3-Way FRET imaging of protein interactions in living cells.

Authors:  Brandon L Scott; Adam D Hoppe
Journal:  Sci Rep       Date:  2015-07-01       Impact factor: 4.379

2.  Coordinated integrin activation by actin-dependent force during T-cell migration.

Authors:  Pontus Nordenfelt; Hunter L Elliott; Timothy A Springer
Journal:  Nat Commun       Date:  2016-10-10       Impact factor: 14.919

3.  Rational engineering of ratiometric calcium sensors with bright green and red fluorescent proteins.

Authors:  Diming Zhang; Emily Redington; Yiyang Gong
Journal:  Commun Biol       Date:  2021-07-29
  3 in total

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