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.
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- Fluorescence Recovery After Photobleaching
- FRAP (Fluorescence Recovery After Photobleaching)
- FRAPs (Fluorescence Recovery After Photobleaching)
- Fluorescence Photobleaching Recovery
|
Below are MeSH descriptors whose meaning is more general than "Fluorescence Recovery After Photobleaching".
Below are MeSH descriptors whose meaning is more specific than "Fluorescence Recovery After Photobleaching".
This graph shows the total number of publications written about "Fluorescence Recovery After Photobleaching" by people in this website by year, and whether "Fluorescence Recovery After Photobleaching" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2002 | 0 | 1 | 1 |
| 2005 | 0 | 1 | 1 |
| 2007 | 0 | 2 | 2 |
| 2008 | 0 | 2 | 2 |
| 2010 | 1 | 1 | 2 |
| 2011 | 0 | 1 | 1 |
| 2012 | 0 | 1 | 1 |
| 2014 | 0 | 1 | 1 |
| 2017 | 0 | 1 | 1 |
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Below are the most recent publications written about "Fluorescence Recovery After Photobleaching" by people in Profiles.
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An amidase is required for proper intercellular communication in the filamentous cyanobacterium Anabaena sp. PCC 7120. Proc Natl Acad Sci U S A. 2017 02 21; 114(8):E1405-E1412.
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Macroglobulin complement-related encodes a protein required for septate junction organization and paracellular barrier function in Drosophila. Development. 2014 Feb; 141(4):889-98.
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Phase transitions in the assembly of multivalent signalling proteins. Nature. 2012 Mar 07; 483(7389):336-40.
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Assembly and maintenance of nodes of ranvier rely on distinct sources of proteins and targeting mechanisms. Neuron. 2012 Jan 12; 73(1):92-107.
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Analysis of protein dynamics within the septate junction reveals a highly stable core protein complex that does not include the basolateral polarity protein Discs large. J Cell Sci. 2011 Aug 15; 124(Pt 16):2861-71.
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Sterile alpha motif domain-mediated self-association plays an essential role in modulating the activity of the Drosophila ETS family transcriptional repressor Yan. Mol Cell Biol. 2010 Mar; 30(5):1158-70.
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The use of fluorescence redistribution after photobleaching for analysis of cellular microtubule dynamics. Methods Cell Biol. 2010; 97:35-52.
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Molecular mechanism of protein assembly on DNA double-strand breaks in the non-homologous end-joining pathway. J Radiat Res. 2009 Mar; 50(2):97-108.
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Neuropeptide FF-sensitive confinement of mu opioid receptor does not involve lipid rafts in SH-SY5Y cells. Biochem Biophys Res Commun. 2008 Aug 15; 373(1):80-4.
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The tight junction protein complex undergoes rapid and continuous molecular remodeling at steady state. J Cell Biol. 2008 May 19; 181(4):683-95.