(Q34405311)

2 August 2017

title

Three-chromophore FRET microscopy to analyze multiprotein interactions in living cells (English)

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2 August 2017

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Emilia Galperin

1

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2 August 2017

Vladislav V Verkhusha

series ordinal

2

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2 August 2017

Alexander Sorkin

series ordinal

3

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2 August 2017

publication date

18 November 2004

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2 August 2017

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2 August 2017

volume

1

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2 August 2017

issue

3

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2 August 2017

page(s)

209-217

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https://scigraph.springernature.com/pub.10.1038/nmeth720

2 August 2017

exact match

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7 January 2021

Creating new fluorescent probes for cell biology.

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Ras signalling on the endoplasmic reticulum and the Golgi

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Imaging sites of receptor dephosphorylation by PTP1B on the surface of the endoplasmic reticulum

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Coordinated traffic of Grb2 and Ras during epidermal growth factor receptor endocytosis visualized in living cells

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Interaction of EGF receptor and grb2 in living cells visualized by fluorescence resonance energy transfer (FRET) microscopy

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Genetically encoded reporters of protein kinase A activity reveal impact of substrate tethering

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Spatio-temporal images of growth-factor-induced activation of Ras and Rap1.

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A genetically encoded fluorescent reporter reveals oscillatory phosphorylation by protein kinase C

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Mechanism of the spatio-temporal regulation of Ras and Rap1.

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Localized Rac activation dynamics visualized in living cells

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Fluorescent proteins from nonbioluminescent Anthozoa species

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Diversity and evolution of the green fluorescent protein family.

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GFP-like chromoproteins as a source of far-red fluorescent proteins

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The molecular properties and applications of Anthozoa fluorescent proteins and chromoproteins.

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A monomeric red fluorescent protein

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Imaging biochemistry inside cells

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Two-step FRET as a structural tool

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Multistep Fluorescence Resonance Energy Transfer in Sequential Chromophore Array Constructed on Oligo-DNA Assemblies

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FRET Study of a Trifluorophore-Labeled DNAzyme

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Using GFP in FRET-based applications

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7 January 2021

Quantitative fluorescence resonance energy transfer measurements using fluorescence microscopy

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7 January 2021

FRET microscopy demonstrates molecular association of non-specific lipid transfer protein (nsL-TP) with fatty acid oxidation enzymes in peroxisomes

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7 January 2021

Divalent Rab effectors regulate the sub-compartmental organization and sorting of early endosomes.

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7 January 2021

Visualization of Rab5 activity in living cells by FRET microscopy and influence of plasma-membrane-targeted Rab5 on clathrin-dependent endocytosis

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7 January 2021

Endocytosis of functional epidermal growth factor receptor-green fluorescent protein chimera

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7 January 2021

Epidermal growth factor receptor internalization through clathrin-coated pits requires Cbl RING finger and proline-rich domains but not receptor polyubiquitylation

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7 January 2021

Grb2 regulates internalization of EGF receptors through clathrin-coated pits

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7 January 2021

A protease assay for two-photon crosscorrelation and FRET analysis based solely on fluorescent proteins

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7 January 2021

Reliable and global measurement of fluorescence resonance energy transfer using fluorescence microscopes

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7 January 2021

FRET or no FRET: a quantitative comparison

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7 January 2021

Identifiers

DOI

10.1038/NMETH720

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Dimensions Publication ID

2 August 2017

1008852774

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