Single-molecule evaluation of fluorescent protein photoactivation efficiency using an in vivo nanotemplate. (Q48611227)

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4 March 2020

title

Single-molecule evaluation of fluorescent protein photoactivation efficiency using an in vivo nanotemplate (English)

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4 March 2020

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1

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4 March 2020

Lara Laparra-Cuervo

series ordinal

2

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4 March 2020

Joseph Steven Borbely

series ordinal

4

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4 March 2020

5

Melike Lakadamyali

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4 March 2020

author name string

Angel Sandoval-Álvarez

series ordinal

3

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4 March 2020

publication date

5 January 2014

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4 March 2020

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4 March 2020

volume

11

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4 March 2020

page(s)

156-162

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4 March 2020

issue

2

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https://scigraph.springernature.com/pub.10.1038/nmeth.2784

4 March 2020

exact match

0 references

cites work

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Ultra-high resolution imaging by fluorescence photoactivation localization microscopy

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Breaking the diffraction barrier: super-resolution imaging of cells

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Whole-cell 3D STORM reveals interactions between cellular structures with nanometer-scale resolution

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3D multicolor super-resolution imaging offers improved accuracy in neuron tracing

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Correlative live-cell and superresolution microscopy reveals cargo transport dynamics at microtubule intersections.

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Nanoscale architecture of integrin-based cell adhesions

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Actin, spectrin, and associated proteins form a periodic cytoskeletal structure in axons

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Quantitative single-molecule microscopy reveals that CENP-A(Cnp1) deposition occurs during G2 in fission yeast.

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Plasticity of the asialoglycoprotein receptor deciphered by ensemble FRET imaging and single-molecule counting PALM imaging

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Probing protein heterogeneity in the plasma membrane using PALM and pair correlation analysis

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

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Structural basis of enhanced photoconversion yield in green fluorescent protein-like protein Dendra2

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Counting bungarotoxin binding sites of nicotinic acetylcholine receptors in mammalian cells with high signal/noise ratios

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Counting molecules in single organelles with superresolution microscopy allows tracking of the endosome maturation trajectory.

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A technical consideration concerning the removal of oocyte vitelline membranes for patch clamp recording.

21 January 2018

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Identification of the factors affecting co-localization precision for quantitative multicolor localization microscopy

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Quantitative Super-Resolution Imaging Reveals Protein Stoichiometry and Nanoscale Morphology of Assembling HIV-Gag Virions

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PubMed

https://pubmed.ncbi.nlm.nih.gov/24390439

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Subunit counting in membrane-bound proteins

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24390439

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/NMETH.2784

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24390439%20AND%20SRC:MED&resulttype=core&format=json

4 March 2020

1 reference