Literature DB >> 34331287

Out-of-Phase Imaging after Optical Modulation (OPIOM) for Multiplexed Fluorescence Imaging Under Adverse Optical Conditions.

Raja Chouket1, Ruikang Zhang1, Agnès Pellissier-Tanon1, Annie Lemarchand2, Agathe Espagne1, Thomas Le Saux3, Ludovic Jullien4.   

Abstract

Fluorescence imaging has become a powerful tool for observations in biology. Yet it has also encountered limitations to overcome optical interferences of ambient light, autofluorescence, and spectrally interfering fluorophores. In this account, we first examine the current approaches which address these limitations. Then we more specifically report on Out-of-Phase Imaging after Optical Modulation (OPIOM), which has proved attractive for highly selective multiplexed fluorescence imaging even under adverse optical conditions. After exposing the OPIOM principle, we detail the protocols for successful OPIOM implementation.
© 2021. Springer Science+Business Media, LLC, part of Springer Nature.

Keywords:  Dynamic contrast; Fluorescence endomicroscopy; Fluorescence imaging; Fluorescence microscopy; Macroscale imaging; Reversibly photoswitchable fluorophores

Year:  2021        PMID: 34331287     DOI: 10.1007/978-1-0716-1593-5_13

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  152 in total

1.  Measuring tubulin content in Toxoplasma gondii: a comparison of laser-scanning confocal and wide-field fluorescence microscopy.

Authors:  Jason R Swedlow; Ke Hu; Paul D Andrews; David S Roos; John M Murray
Journal:  Proc Natl Acad Sci U S A       Date:  2002-02-05       Impact factor: 11.205

2.  Rapid, noninvasive screening for perturbations of metabolism and plant growth using chlorophyll fluorescence imaging.

Authors:  Romina P Barbagallo; Kevin Oxborough; Kenneth E Pallett; Neil R Baker
Journal:  Plant Physiol       Date:  2003-06       Impact factor: 8.340

3.  Kinetic imaging of chlorophyll fluorescence using modulated light.

Authors:  L Nedbal; J Soukupová; D Kaftan; J Whitmarsh; M Trtílek
Journal:  Photosynth Res       Date:  2000       Impact factor: 3.573

Review 4.  The fluorescent toolbox for assessing protein location and function.

Authors:  Ben N G Giepmans; Stephen R Adams; Mark H Ellisman; Roger Y Tsien
Journal:  Science       Date:  2006-04-14       Impact factor: 47.728

Review 5.  Monitoring and screening plant populations with combined thermal and chlorophyll fluorescence imaging.

Authors:  Laury Chaerle; Ilkka Leinonen; Hamlyn G Jones; Dominique Van Der Straeten
Journal:  J Exp Bot       Date:  2006-12-22       Impact factor: 6.992

6.  Autofluorescence of viable cultured mammalian cells.

Authors:  J E Aubin
Journal:  J Histochem Cytochem       Date:  1979-01       Impact factor: 2.479

7.  Thermal and chlorophyll-fluorescence imaging distinguish plant-pathogen interactions at an early stage.

Authors:  Laury Chaerle; Dik Hagenbeek; Erik De Bruyne; Roland Valcke; Dominique Van Der Straeten
Journal:  Plant Cell Physiol       Date:  2004-07       Impact factor: 4.927

8.  Accuracy and precision in quantitative fluorescence microscopy.

Authors:  Jennifer C Waters
Journal:  J Cell Biol       Date:  2009-06-29       Impact factor: 10.539

9.  Pulsed-light imaging for fluorescence guided surgery under normal room lighting.

Authors:  Kristian Sexton; Scott C Davis; David McClatchy; Pablo A Valdes; Stephen C Kanick; Keith D Paulsen; David W Roberts; Brian W Pogue
Journal:  Opt Lett       Date:  2013-09-01       Impact factor: 3.776

10.  Evaluating performance in three-dimensional fluorescence microscopy.

Authors:  John M Murray; Paul L Appleton; Jason R Swedlow; Jennifer C Waters
Journal:  J Microsc       Date:  2007-12       Impact factor: 1.758

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