| Title | Molecular imaging. | | Author(s) | Konietzny R, König A, Wotzlaw C, Bernadini A, Berchner-Pfannschmidt U, Fandrey J | | Institution | Institute for Physiology, University of Duisburg-Essen, Essen, Germany. | | Source | Ann N Y Acad Sci 2009 Oct.:74-81. | | Abstract | Fluorescence resonance energy transfer (FRET) combined with confocal laser microscopy is a powerful tool to analyze protein-protein interaction in vivo. We have applied this combination to study the assembly of the hypoxia-inducible factor (HIF) complex in living cells under hypoxic conditions. In hypoxia, the basic helix-loop-helix/Period/ARNT/Single-minded (PAS) proteins HIF-1alpha and HIF-2alpha accumulate and are translocated into the nucleus. Here, HIF-1alpha and HIF-2alpha dimerize with HIF-1beta, also known as aryl hydrocarbon receptor nuclear translocator (ARNT), to form HIF-1/HIF-2 complexes, which control the expression of specific target genes. Therefore, a new Java-based analyzing program was developed at our institute to calculate the nanometer distance between alpha and beta subunits of the transcriptionally active HIF-1/-2 complex bound to DNA. Fusion proteins of HIF subunits and variants of green fluorescent proteins (cyan and yellow fluorescent proteins) were expressed in living cells and protein-protein interactions were imaged in vivo by means of FRET. | | Language | eng | | Pub Type(s) | Journal Article
| | PubMed ID | 19845609 |
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