Literature DB >> 19566331

Enhanced yellow fluorescent protein photoconversion to a cyan fluorescent protein-like species is sensitive to thermal and diffusion conditions.

Merete K Raarup1, Anja W Fjorback, Stig M R Jensen, Heidi K Müller, Maj M Kjaergaard, Hanne Poulsen, Ove Wiborg, Jens R Nyengaard.   

Abstract

Ongoing research efforts into fluorescent proteins continuously generates new mutation variants, some of which can become photoactivated or photoconverted to a red-shifted color upon intense UV or blue light illumination. We report a built-in propensity for enhanced yellow fluorescent protein (EYFP) to undergo irreversible photoconversion into a cyan fluorescent protein (CFP)-like species upon green-light illumination. The photoconversion is thermally activated, happens mainly in fixed, nonsealed cell samples, and may result in a very bright and relatively photostable CFP-like species. The photoconversion efficiency depends on the sample diffusivity and is much increased in dehydrated, oxygenated samples. Given the large variations in conversion efficiency observed among samples as well as within a sample, photoconversion cannot be appropriately accounted for in the analysis of acceptor photobleaching fluorescence resonance energy transfer (pbFRET) images and should rather be completely avoided. Thus, samples should always be checked and discarded if photoconversion is observed.

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Year:  2009        PMID: 19566331     DOI: 10.1117/1.3103338

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


  6 in total

1.  Some secrets of fluorescent proteins: distinct bleaching in various mounting fluids and photoactivation of cyan fluorescent proteins at YFP-excitation.

Authors:  Naila Malkani; Johannes A Schmid
Journal:  PLoS One       Date:  2011-04-07       Impact factor: 3.240

Review 2.  Quantification of Förster resonance energy transfer by monitoring sensitized emission in living plant cells.

Authors:  Sara M Müller; Helena Galliardt; Jessica Schneider; B George Barisas; Thorsten Seidel
Journal:  Front Plant Sci       Date:  2013-10-29       Impact factor: 5.753

3.  Improving brightness and photostability of green and red fluorescent proteins for live cell imaging and FRET reporting.

Authors:  Bryce T Bajar; Emily S Wang; Amy J Lam; Bongjae B Kim; Conor L Jacobs; Elizabeth S Howe; Michael W Davidson; Michael Z Lin; Jun Chu
Journal:  Sci Rep       Date:  2016-02-16       Impact factor: 4.379

Review 4.  Single-molecule fluorescence microscopy review: shedding new light on old problems.

Authors:  Sviatlana Shashkova; Mark C Leake
Journal:  Biosci Rep       Date:  2017-07-21       Impact factor: 3.840

5.  Flow cytometry-based FRET identifies binding intensities in PPARγ1 protein-protein interactions in living cells.

Authors:  Verena Trümper; Andreas von Knethen; Annegret Preuß; Eugeny Ermilov; Steffen Hackbarth; Laura Kuchler; Sandra Gunne; Anne Schäfer; Tobias Bornhütter; György Vereb; Lázló Ujlaky-Nagy; Bernhard Brüne; Beate Röder; Michael Schindler; Michael J Parnham; Tilo Knape
Journal:  Theranostics       Date:  2019-07-28       Impact factor: 11.556

6.  Improving FRET dynamic range with bright green and red fluorescent proteins.

Authors:  Amy J Lam; François St-Pierre; Yiyang Gong; Jesse D Marshall; Paula J Cranfill; Michelle A Baird; Michael R McKeown; Jörg Wiedenmann; Michael W Davidson; Mark J Schnitzer; Roger Y Tsien; Michael Z Lin
Journal:  Nat Methods       Date:  2012-09-09       Impact factor: 28.547

  6 in total

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