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J Biomol Screen ; 8(1): 19-33, 2003 Feb.
Article in English | MEDLINE | ID: mdl-12854995

ABSTRACT

Single-molecule detection technologies are becoming a powerful readout format to support ultra-high-throughput screening. These methods are based on the analysis of fluorescence intensity fluctuations detected from a small confocal volume element. The fluctuating signal contains information about the mass and brightness of the different species in a mixture. The authors demonstrate a number of applications of fluorescence intensity distribution analysis (FIDA), which discriminates molecules by their specific brightness. Examples for assays based on brightness changes induced by quenching/dequenching of fluorescence, fluorescence energy transfer, and multiple-binding stoichiometry are given for important drug targets such as kinases and proteases. FIDA also provides a powerful method to extract correct biological data in the presence of compound fluorescence.


Subject(s)
Microscopy, Confocal , Alcohol Dehydrogenase/analysis , Alkaline Phosphatase/analysis , Antigens, Human Platelet/analysis , Antigens, Human Platelet/metabolism , Endopeptidases/analysis , Endopeptidases/metabolism , Fluorescence , Ligands , RNA/metabolism
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