(Q34664023)

3 August 2017

title

Tracking intracellular protein movements using photoswitchable fluorescent proteins PS-CFP2 and Dendra2. (English)

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3 August 2017

Dmitriy M Chudakov

1

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author name string

Sergey Lukyanov

series ordinal

2

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3 August 2017

Konstantin A Lukyanov

series ordinal

3

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3 August 2017

publication date

1 January 2007

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3 August 2017

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3 August 2017

volume

2

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3 August 2017

issue

8

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3 August 2017

page(s)

2024-2032

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https://scigraph.springernature.com/pub.10.1038/nprot.2007.291

3 August 2017

exact match

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cites work

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Phototransformation of green fluorescent protein with UV and visible light leads to decarboxylation of glutamate 222

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Engineering of a monomeric green-to-red photoactivatable fluorescent protein induced by blue light

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Photo-induced peptide cleavage in the green-to-red conversion of a fluorescent protein.

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Natural animal coloration can Be determined by a nonfluorescent green fluorescent protein homolog

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Chromophore environment provides clue to "kindling fluorescent protein" riddle

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Regulated fast nucleocytoplasmic shuttling observed by reversible protein highlighting

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Structural basis for reversible photobleaching of a green fluorescent protein homologue

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Structural basis for reversible photoswitching in Dronpa

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Wide-field subdiffraction RESOLFT microscopy using fluorescent protein photoswitching.

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Imaging intracellular fluorescent proteins at nanometer resolution

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Fluorescent proteins as a toolkit for in vivo imaging

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An in vivo comparison of photoactivatable fluorescent proteins in an avian embryo model

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1.8 A bright-state structure of the reversibly switchable fluorescent protein Dronpa guides the generation of fast switching variants

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Identifiers

DOI

10.1038/NPROT.2007.291

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Dimensions Publication ID

3 August 2017

1040567939

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1 reference