Fluorescence Polarization
"Fluorescence Polarization" 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.
Measurement of the polarization of fluorescent light from solutions or microscopic specimens. It is used to provide information concerning molecular size, shape, and conformation, molecular anisotropy, electronic energy transfer, molecular interaction, including dye and coenzyme binding, and the antigen-antibody reaction.
Descriptor ID |
D005454
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MeSH Number(s) |
E05.196.712.516.600.390
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Concept/Terms |
Fluorescence Polarization- Fluorescence Polarization
- Polarization, Fluorescence
- Fluorescence Polarizations
- Polarizations, Fluorescence
Anisotropy, Fluorescence- Anisotropy, Fluorescence
- Anisotropies, Fluorescence
- Fluorescence Anisotropies
- Fluorescence Anisotropy
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Below are MeSH descriptors whose meaning is more general than "Fluorescence Polarization".
Below are MeSH descriptors whose meaning is more specific than "Fluorescence Polarization".
This graph shows the total number of publications written about "Fluorescence Polarization" by people in this website by year, and whether "Fluorescence Polarization" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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1995 | 0 | 1 | 1 |
2008 | 1 | 1 | 2 |
2009 | 0 | 1 | 1 |
2010 | 0 | 1 | 1 |
2012 | 1 | 0 | 1 |
2014 | 0 | 1 | 1 |
2016 | 0 | 1 | 1 |
2023 | 0 | 1 | 1 |
2024 | 1 | 0 | 1 |
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Below are the most recent publications written about "Fluorescence Polarization" by people in Profiles.
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GS-441524-Diphosphate-Ribose Derivatives as Nanomolar Binders and Fluorescence Polarization Tracers for SARS-CoV-2 and Other Viral Macrodomains. ACS Chem Biol. 2024 05 17; 19(5):1093-1105.
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A Fluorescence Polarization Assay for Macrodomains Facilitates the Identification of Potent Inhibitors of the SARS-CoV-2 Macrodomain. ACS Chem Biol. 2023 05 19; 18(5):1200-1207.
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Dissection of molecular assembly dynamics by tracking orientation and position of single molecules in live cells. Proc Natl Acad Sci U S A. 2016 10 18; 113(42):E6352-E6361.
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Allosteric inhibition of the neuropeptidase neurolysin. J Biol Chem. 2014 Dec 19; 289(51):35605-19.
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Enhanced prediction of Src homology 2 (SH2) domain binding potentials using a fluorescence polarization-derived c-Met, c-Kit, ErbB, and androgen receptor interactome. Mol Cell Proteomics. 2014 Jul; 13(7):1705-23.
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Comprehensive binary interaction mapping of SH2 domains via fluorescence polarization reveals novel functional diversification of ErbB receptors. PLoS One. 2012; 7(9):e44471.
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Artemis C-terminal region facilitates V(D)J recombination through its interactions with DNA Ligase IV and DNA-PKcs. J Exp Med. 2012 May 07; 209(5):955-63.
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Holo-Ni(II)HpNikR is an asymmetric tetramer containing two different nickel-binding sites. J Am Chem Soc. 2010 Oct 20; 132(41):14447-56.
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Avid interactions underlie the Lys63-linked polyubiquitin binding specificities observed for UBA domains. Nat Struct Mol Biol. 2009 Aug; 16(8):883-9.
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Aryl acid adenylating enzymes involved in siderophore biosynthesis: fluorescence polarization assay, ligand specificity, and discovery of non-nucleoside inhibitors via high-throughput screening. Biochemistry. 2008 Nov 11; 47(45):11735-49.