High-contrast imaging of fluorescent protein FRET by fluorescence polarization microscopy

Mark A. Rizzo, David W. Piston

Research output: Contribution to journalArticle

96 Scopus citations

Abstract

Detection of Förster resonance energy transfer (FRET) between fluorescent protein labeled targets is a valuable strategy for measurement of protein-protein interactions and other intracellular processes. Despite the utility of FRET, widespread application of this technique to biological problems and high-throughput screening has been limited by low-contrast measurement strategies that rely on the detection of sensitized emission or photodestruction of the sample. Here we report a FRET detection strategy based on detecting depolarized sensitized emission. In the absence of FRET, we show that fluorescence emission from a donor fluorescent protein is highly polarized. Depolarization of fluorescence emission is observed only in the presence of energy transfer. A simple detection strategy was adapted for fluorescence microscopy using both laser scanning and wide-field approaches. This approach is able to distinguish FRET between linked and unlinked Cerulean and Venus fluorescent proteins in living cells with a larger dynamic range than other approaches.

Original languageEnglish
Pages (from-to)L14-L16
JournalBiophysical Journal
Volume88
Issue number2
DOIs
StatePublished - Feb 2005
Externally publishedYes

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