Use of [125I]4′-iodoflavone as a tool to characterize ligand-dependent differences in Ah receptor behavior

Hollie I. Swanson, Murray L. Whitelaw, John R. Petrulis, Gary H. Perdew

Research output: Contribution to journalReview article

5 Scopus citations

Abstract

We have synthesized [125I]4′-iodoflavone to study Ah receptor (AhR)-ligand interactions by a class of AhR ligands distinct from the prototypic ligand 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD). This radioligand allows the comparison of AhR-ligand interactions using a ligand that differs in AhR affinity, and yet has the same radiospecific activity as [125I]2-iodo-7,8-dibromodibenzo-p-dioxin. Specific binding of [125I]4′-iodoflavone with the AhR was detected as a single radioactive peak (∼9.7 S) following density sucrose gradient analysis. Cytosolic extracts from both Hepa 1 and HeLa cells were used as the source of mouse and human AhR, respectively. A ∼6.7 S form of radioligand-bound Ah receptor was detected in the high salt nuclear extracts of both cell lines. In HeLa cells approximately twofold more [125I]4′-iodoflavone-AhR 6 S complex, compared with [125I]2-iodo-7,8-dibromodibenzo-p-dioxin, was recovered in nuclear extracts. A comparison of the ability of 4′-iodoflavone and TCDD to cause time-dependent translocation of AhR-yellow fluorescent protein revealed that 4′-iodoflavone was more efficient at enhancing nuclear accumulation of the receptor. These results suggest that [125I]4′-iodoflavone is a particularly useful and easily synthesized ligand for studying the AhR.

Original languageEnglish (US)
Pages (from-to)298-310
Number of pages13
JournalJournal of Biochemical and Molecular Toxicology
Volume16
Issue number6
DOIs
StatePublished - Dec 1 2002

All Science Journal Classification (ASJC) codes

  • Biochemistry
  • Molecular Medicine
  • Molecular Biology
  • Toxicology
  • Health, Toxicology and Mutagenesis

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