Direct measurement of protein dynamics inside cells using a rationally designed photoconvertible protein (Q50642586)

17 March 2018

title

Direct measurement of protein dynamics inside cells using a rationally designed photoconvertible protein (English)

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17 March 2018

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Tomoki Matsuda

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17 March 2018

Atsushi Miyawaki

series ordinal

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17 March 2018

Takeharu Nagai

series ordinal

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17 March 2018

publication date

16 March 2008

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17 March 2018

published in

Nature Methods

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17 March 2018

volume

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17 March 2018

issue

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17 March 2018

page(s)

339-345

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17 March 2018

Studying protein dynamics in living cells

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

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High mobility of proteins in the mammalian cell nucleus

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Measurement of cytosolic, mitochondrial, and Golgi pH in single living cells with green fluorescent proteins

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Global chromosome positions are transmitted through mitosis in mammalian cells

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Microenvironment and effect of energy depletion in the nucleus analyzed by mobility of multiple oligomeric EGFPs

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Intracellular macromolecular mobility measured by fluorescence recovery after photobleaching with confocal laser scanning microscopes.

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Fluorescence recovery after photobleaching: a versatile tool for mobility and interaction measurements in pharmaceutical research

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The intranuclear mobility of messenger RNA binding proteins is ATP dependent and temperature sensitive

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Mobility measurement by analysis of fluorescence photobleaching recovery kinetics

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inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/NMETH.1193

1 reference

17 March 2018

1 reference

17 March 2018