Literature DB >> 16964606

A green to red photoconvertible protein as an analyzing tool for early vertebrate development.

Stephan A Wacker1, Franz Oswald, Jörg Wiedenmann, Walter Knöchel.   

Abstract

Lineage labeling is one of the most important techniques in developmental biology. Most recently, a set of photoactivatable fluorescent proteins originating from marine cnidarians became available. Here, we introduce the application of the green to red photoconvertible protein EosFP as a novel technique to analyze early vertebrate development. Both injection of EosFP mRNA and purified, recombinant EosFP followed by a light-driven green to red conversion allow lineage labeling in virtually any temporal and spatial dimension during embryonic development for at least 2 weeks. Specific staining of cells from nonsurface layers is greatly facilitated by light-driven conversion of EosFP compared with traditional methods. Therefore, green to red photoactivatable proteins promise to be a powerful tool with the potential to satisfy the increasing demand for methods enabling detailed phenotypical analyses after manipulations of morphogenetic events, gene expression, or signal transduction.

Mesh:

Substances:

Year:  2007        PMID: 16964606     DOI: 10.1002/dvdy.20955

Source DB:  PubMed          Journal:  Dev Dyn        ISSN: 1058-8388            Impact factor:   3.780


  24 in total

1.  Photoconversion for tracking the dynamics of cell movement in Xenopus laevis embryos.

Authors:  Brook T Chernet; Dany S Adams; Michael Levin
Journal:  Cold Spring Harb Protoc       Date:  2012-06-01

2.  Photomodulatable fluorescent proteins for imaging cell dynamics and cell fate.

Authors:  Sonja Nowotschin; Anna-Katerina Hadjantonakis
Journal:  Organogenesis       Date:  2009-10       Impact factor: 2.500

3.  Watching the assembly of an organ a single cell at a time using confocal multi-position photoactivation and multi-time acquisition.

Authors:  Paul M Kulesa; Danny A Stark; Joseph Steen; Rusty Lansford; Jennifer C Kasemeier-Kulesa
Journal:  Organogenesis       Date:  2009-10       Impact factor: 2.500

4.  Neural crest invasion is a spatially-ordered progression into the head with higher cell proliferation at the migratory front as revealed by the photoactivatable protein, KikGR.

Authors:  Paul M Kulesa; Jessica M Teddy; Danny A Stark; Sarah E Smith; Rebecca McLennan
Journal:  Dev Biol       Date:  2008-02-07       Impact factor: 3.582

5.  A crystallographic study of bright far-red fluorescent protein mKate reveals pH-induced cis-trans isomerization of the chromophore.

Authors:  Sergei Pletnev; Dmitry Shcherbo; Dmitry M Chudakov; Nadezhda Pletneva; Ekaterina M Merzlyak; Alexander Wlodawer; Zbigniew Dauter; Vladimir Pletnev
Journal:  J Biol Chem       Date:  2008-08-04       Impact factor: 5.157

6.  Control of local protein synthesis and initial events in myelination by action potentials.

Authors:  Hiroaki Wake; Philip R Lee; R Douglas Fields
Journal:  Science       Date:  2011-08-04       Impact factor: 47.728

7.  Tracking single proteins in live cells using single-chain antibody fragment-fluorescent quantum dot affinity pair.

Authors:  Gopal Iyer; Xavier Michalet; Yun-Pei Chang; Shimon Weiss
Journal:  Methods Enzymol       Date:  2010       Impact factor: 1.600

8.  LlamaTags: A Versatile Tool to Image Transcription Factor Dynamics in Live Embryos.

Authors:  Jacques P Bothma; Matthew R Norstad; Simon Alamos; Hernan G Garcia
Journal:  Cell       Date:  2018-05-10       Impact factor: 41.582

Review 9.  Photoactivatable fluorescent proteins for diffraction-limited and super-resolution imaging.

Authors:  Jennifer Lippincott-Schwartz; George H Patterson
Journal:  Trends Cell Biol       Date:  2009-11       Impact factor: 20.808

10.  Use of KikGR a photoconvertible green-to-red fluorescent protein for cell labeling and lineage analysis in ES cells and mouse embryos.

Authors:  Sonja Nowotschin; Anna-Katerina Hadjantonakis
Journal:  BMC Dev Biol       Date:  2009-09-09       Impact factor: 1.978

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