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Fluorescence Polarization (FP) Assays for Monitoring Peptide-Protein or Nucleic Acid-Protein Binding.

Authors :
Moerke NJ
Source :
Current protocols in chemical biology [Curr Protoc Chem Biol] 2009 Dec 01; Vol. 1 (1), pp. 1-15.
Publication Year :
2009

Abstract

The technique of fluorescence polarization (FP) is based on the observation that when a fluorescently labeled molecule is excited by polarized light, it emits light with a degree of polarization that is inversely proportional to the rate of molecular rotation. This property of fluorescence can be used to measure the interaction of a small labeled ligand with a larger protein and provides a basis for direct and competition binding assays. FP assays are readily adaptable to a high-throughput format, have been used successfully in screens directed against a wide range of targets, and are particularly valuable in screening for inhibitors of protein-protein and protein-nucleic acid interactions when a small binding epitope can be identified for one of the partners. The protocols in this article describe a general procedure for development of FP assays to monitor binding of such a peptide or oligonucleotide to a protein of interest. Curr. Protoc. Chem Biol. 1:1-15. © 2009 by John Wiley & Sons, Inc.

Details

Language :
English
ISSN :
2160-4762
Volume :
1
Issue :
1
Database :
MEDLINE
Journal :
Current protocols in chemical biology
Publication Type :
Academic Journal
Accession number :
23839960
Full Text :
https://doi.org/10.1002/9780470559277.ch090102