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- W47411888 abstract "Publisher Summary The measurement of fluorescence resonance energy transfer (FRET) between variants of fluorescent proteins has emerged as a powerful tool for intracellular measurements of protein reactions. FRET cannot be measured directly, but its occurrence is reflected by changes in the fluorescence kinetics of both the donor and the acceptor molecules that can be measured by optical means. FRET reduces the fluorescence lifetime of the donor molecule since it depopulates its excited state. Thus, the measurement of the fluorescence lifetime of the donor can be used as an indicator for FRET. In such an assay, the donor–acceptor pair is chosen such that the donor fluorescence can be detected specifically without detecting any acceptor fluorescence. The use of green fluorescent protein variants as partners in a FRET pair requires consideration of the relative expression levels of the two-protein GFP fusions in the light of the measurement method that is being used. The data analysis steps for sensitized emission measurements are fairly simple and can be performed with many commercially available image processing packages." @default.
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- W47411888 date "2006-01-01" @default.
- W47411888 modified "2023-09-25" @default.
- W47411888 title "Imaging Fluorescence Resonance Energy Transfer between Green Fluorescent Protein Variants in Live Cells" @default.
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- W47411888 doi "https://doi.org/10.1016/b978-012164730-8/50143-x" @default.
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