Fluorescence Recovery After Photobleaching

"Fluorescence Recovery After Photobleaching" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

MeSH information

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A method used to study the lateral movement of MEMBRANE PROTEINS and LIPIDS. A small area of a cell membrane is bleached by laser light and the amount of time necessary for unbleached fluorescent marker-tagged proteins to diffuse back into the bleached site is a measurement of the cell membrane's fluidity. The diffusion coefficient of a protein or lipid in the membrane can be calculated from the data. (From Segen, Current Med Talk, 1995).

Descriptor ID

D036681

MeSH Number(s)

E05.196.712.516.600.393

Concept/Terms

Fluorescence Recovery After Photobleaching

Below are MeSH descriptors whose meaning is more general than "Fluorescence Recovery After Photobleaching".

Analytical, Diagnostic and Therapeutic Techniques and Equipment [E]
Investigative Techniques [E05]
Chemistry Techniques, Analytical [E05.196]
Photometry [E05.196.712]
Luminescent Measurements [E05.196.712.516]
Fluorometry [E05.196.712.516.600]
Fluorescence Recovery After Photobleaching [E05.196.712.516.600.393]

Below are MeSH descriptors whose meaning is related to "Fluorescence Recovery After Photobleaching".

Below are MeSH descriptors whose meaning is more specific than "Fluorescence Recovery After Photobleaching".

publications

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This graph shows the total number of publications written about "Fluorescence Recovery After Photobleaching" by people in Harvard Catalyst Profiles by year, and whether "Fluorescence Recovery After Photobleaching" was a major or minor topic of these publication.

Below are the most recent publications written about "Fluorescence Recovery After Photobleaching" by people in Profiles.

Measurement of Protein and Nucleic Acid Diffusion Coefficients Within Biomolecular Condensates Using In-Droplet Fluorescence Correlation Spectroscopy. Methods Mol Biol. 2023; 2563:199-213.

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Real-time visualization of titin dynamics reveals extensive reversible photobleaching in human induced pluripotent stem cell-derived cardiomyocytes. Am J Physiol Cell Physiol. 2020 01 01; 318(1):C163-C173.

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Divalent cations can control a switch-like behavior in heterotypic and homotypic RNA coacervates. Sci Rep. 2019 08 21; 9(1):12161.

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The Kinetics of Nucleotide Binding to Isolated Chlamydomonas Axonemes Using UV-TIRF Microscopy. Biophys J. 2019 08 20; 117(4):679-687.

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Axonal G3BP1 stress granule protein limits axonal mRNA translation and nerve regeneration. Nat Commun. 2018 08 22; 9(1):3358.

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Coactivator condensation at super-enhancers links phase separation and gene control. Science. 2018 07 27; 361(6400).

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Analysis of NTPDase2 in the cell membrane using fluorescence recovery after photobleaching (FRAP). Cytometry A. 2018 02; 93(2):232-238.

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SUMOylation of human septins is critical for septin filament bundling and cytokinesis. J Cell Biol. 2017 12 04; 216(12):4041-4052.

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Local Nucleation of Microtubule Bundles through Tubulin Concentration into a Condensed Tau Phase. Cell Rep. 2017 Sep 05; 20(10):2304-2312.

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The role of a conserved membrane proximal cysteine in altering aPS2CßPS integrin diffusion. Phys Biol. 2016 11 15; 13(6):066005.

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