A bioluminescence resonance energy transfer (BRET) system: application to interacting circadian clock proteins.

Xu Y, Piston DW, Johnson CH
Proc Natl Acad Sci U S A. 1999 96 (1): 151-6

PMID: 9874787 · PMCID: PMC15108 · DOI:10.1073/pnas.96.1.151

We describe a method for assaying protein interactions that offers some attractive advantages over previous assays. This method, called bioluminescence resonance energy transfer (BRET), uses a bioluminescent luciferase that is genetically fused to one candidate protein, and a green fluorescent protein mutant fused to another protein of interest. Interactions between the two fusion proteins can bring the luciferase and green fluorescent protein close enough for resonance energy transfer to occur, thus changing the color of the bioluminescent emission. By using proteins encoded by circadian (daily) clock genes from cyanobacteria, we use the BRET technique to demonstrate that the clock protein KaiB interacts to form homodimers. BRET should be particularly useful for testing protein interactions within native cells, especially with integral membrane proteins or proteins targeted to specific organelles.

MeSH Terms (15)

Bacterial Proteins Biological Clocks Circadian Rhythm Circadian Rhythm Signaling Peptides and Proteins Cloning, Molecular Cyanobacteria Dimerization Energy Transfer Escherichia coli Luciferases Luminescent Measurements Luminescent Proteins Protein Binding Recombinant Fusion Proteins Spectrometry, Fluorescence

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