Literature DB >> 20940350

mEosFP-based green-to-red photoconvertible subcellular probes for plants.

Jaideep Mathur1, Resmi Radhamony, Alison M Sinclair, Ana Donoso, Natalie Dunn, Elyse Roach, Devon Radford, P S Mohammad Mohaghegh, David C Logan, Ksenija Kokolic, Neeta Mathur.   

Abstract

Photoconvertible fluorescent proteins (FPs) are recent additions to the biologists' toolbox for understanding the living cell. Like green fluorescent protein (GFP), monomeric EosFP is bright green in color but is efficiently photoconverted into a red fluorescent form using a mild violet-blue excitation. Here, we report mEosFP-based probes that localize to the cytosol, plasma membrane invaginations, endosomes, prevacuolar vesicles, vacuoles, the endoplasmic reticulum, Golgi bodies, mitochondria, peroxisomes, and the two major cytoskeletal elements, filamentous actin and cortical microtubules. The mEosFP fusion proteins are smaller than GFP/red fluorescent protein-based probes and, as demonstrated here, provide several significant advantages for imaging of living plant cells. These include an ability to differentially color label a single cell or a group of cells in a developing organ, selectively highlight a region of a cell or a subpopulation of organelles and vesicles within a cell for tracking them, and understanding spatiotemporal aspects of interactions between similar as well as different organelles. In addition, mEosFP probes introduce a milder alternative to fluorescence recovery after photobleaching, whereby instead of photobleaching, photoconversion followed by recovery of green fluorescence can be used for estimating subcellular dynamics. Most importantly, the two fluorescent forms of mEosFP furnish bright internal controls during imaging experiments and are fully compatible with cyan fluorescent protein, GFP, yellow fluorescent protein, and red fluorescent protein fluorochromes for use in simultaneous, multicolor labeling schemes. Photoconvertible mEosFP-based subcellular probes promise to usher in a much higher degree of precision to live imaging of plant cells than has been possible so far using single-colored FPs.

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Year:  2010        PMID: 20940350      PMCID: PMC2996014          DOI: 10.1104/pp.110.165431

Source DB:  PubMed          Journal:  Plant Physiol        ISSN: 0032-0889            Impact factor:   8.340


  70 in total

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Review 5.  The endosomal system of plants: charting new and familiar territories.

Authors:  David G Robinson; Liwen Jiang; Karin Schumacher
Journal:  Plant Physiol       Date:  2008-08       Impact factor: 8.340

6.  Random GFP::cDNA fusions enable visualization of subcellular structures in cells of Arabidopsis at a high frequency.

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  23 in total

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Review 6.  Stromules: Probing Formation and Function.

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7.  Color recovery after photoconversion of H2B::mEosFP allows detection of increased nuclear DNA content in developing plant cells.

Authors:  Michael Wozny; Martin H Schattat; Neeta Mathur; Kiah Barton; Jaideep Mathur
Journal:  Plant Physiol       Date:  2011-11-22       Impact factor: 8.340

Review 8.  Applications of phototransformable fluorescent proteins for tracking the dynamics of cellular components.

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Journal:  Plant Physiol       Date:  2014-08-27       Impact factor: 8.340

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