ISI Web of Knowledge Take the next step  
Web of Science®
 
Previous Record (inactive) Record 1  of  1 Next Record (inactive)
Record from Web of Science®
STABLE FLUORESCENT DYE-DNA COMPLEXES IN HIGH-SENSITIVITY DETECTION OF PROTEIN-DNA INTERACTIONS - APPLICATION TO HEAT-SHOCK TRANSCRIPTION FACTOR
Author(s): RYE HS, DREES BL, NELSON HCM, GLAZER AN
Source: JOURNAL OF BIOLOGICAL CHEMISTRY    Volume: 268    Issue: 33    Pages: 25229-25238    Published: NOV 25 1993  
Times Cited: 29     References: 57     
Abstract: The gel mobility-shift assay is an important tool for the study of protein-nucleic acid interactions. High detection sensitivity is typically attained by radioisotopic labeling of the target nucleic acid fragments. A novel fluorescence methology offers significant advantages over this conventional approach. Ethidium, thiazole orange, and oxazole yellow homodimers form stable, highly fluorescent complexes with double-stranded DNA that can be detected in gels by a laser-excited, confocal, fluorescence scanning system with a sensitivity higher than that attainable with radioisotopic labeling. We describe here the use of these dyes in a gel-mobility assay to detect complexes of a truncation of the Kluyveromyces lactis heat shock transcription factor, containing the trimerization and DNA-binding domains (HSF(DT)), with target DNA. At an appropriate molar DNA base pair to dye ratio, the labeling of a DNA fragment with dimeric dye did not affect the binding to HSF(DT). The detection of the fluorescent-dye labeled HSF(DT)-DNA complexes with the laser scanner achieves a spatial resolution far superior to that of conventional autoradiography and permits analysis of multimer protein-DNA complexes that are not resolved by traditional detection methods. We have used this technique to demonstrate that HSF forms multimeric complexes on DNA by addition of trimeric units. The latter conclusion is based on an analysis of the mobilities of the multiple HSF(DT)-DNA complexes and on a two-color mobility-shift fluorescence assay that uses a mutant of HSF(DT) engineered for site-specific labeling with fluorescein and target DNA labeled with an ''energy transfer'' dye, thiazole orange-thiazole blue heterodimer.
Document Type: Article
Language: English
Addresses:
1. UNIV CALIF BERKELEY, DEPT MOLEC & CELL BIOL, DIV BIOCHEM & MOLEC BIOL, BERKELEY, CA 94720 USA
Publisher: AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC, 9650 ROCKVILLE PIKE, BETHESDA, MD 20814
Subject Category: Biochemistry & Molecular Biology
IDS Number: MG673
ISSN: 0021-9258
Previous Record (inactive) Record 1  of  1 Next Record (inactive)
Record from Web of Science®
  
Thomson Reuters Logo