15-deoxy-delta(12-14)-prostaglandin-j2 and 1-anilino-8-naphthalenesulfonate

15-deoxy-delta(12-14)-prostaglandin-j2 has been researched along with 1-anilino-8-naphthalenesulfonate* in 1 studies

Other Studies

1 other study(ies) available for 15-deoxy-delta(12-14)-prostaglandin-j2 and 1-anilino-8-naphthalenesulfonate

ArticleYear
Selective binding of the fluorescent dye 1-anilinonaphthalene-8-sulfonic acid to peroxisome proliferator-activated receptor gamma allows ligand identification and characterization.
    Analytical biochemistry, 2010, Apr-01, Volume: 399, Issue:1

    Peroxisome proliferator-activated receptor gamma (PPARgamma) is a member of the nuclear receptor superfamily involved in insulin sensitization, atherosclerosis, inflammation, and carcinogenesis. PPARgamma transcriptional activity is modulated by specific ligands that promote conformational changes allowing interaction with coactivators. Here we show that the fluorophore 1-anilinonaphthalene-8-sulfonic acid (ANS) binds to PPARgamma-LBD (ligand binding domain), displaying negligible interaction with other nuclear receptors such as PPARalpha and retinoid X receptor alpha (RXRalpha). ANS binding is competed by PPARgamma agonists such as rosiglitazone, 15-deoxy-Delta(12,14)-prostaglandin J(2) (15d-PGJ(2)), and 9,10-dihydro-15-deoxy-Delta(12,14)-prostaglandin J(2) (CAY10410). Moreover, the affinity of PPARgamma for these ligands, determined through ANS competition titrations, is within the range of that reported previously, thereby suggesting that ANS competition could be useful in the screening and characterization of novel PPARgamma agonists. In contrast, gel-based competition assays showed limited performance with noncovalently bound ligands. We applied the ANS binding assay to characterize a biotinylated analog of 15d-PGJ(2) that does not activate PPAR in cells. We found that although this compound bound to PPARgamma with low affinity, it failed to promote PPARgamma interaction with a fluorescent SRC-1 peptide, indicating a lack of receptor activation. Therefore, combined approaches using ANS and fluorescent coactivator peptides to monitor PPARgamma binding and interactions may provide valuable strategies to fully understand the role of PPARgamma ligands.

    Topics: Anilino Naphthalenesulfonates; Binding, Competitive; Fluorescence Polarization; Fluorescent Dyes; Humans; Ligands; PPAR gamma; Prostaglandin D2; Protein Binding; Protein Structure, Tertiary; Recombinant Proteins; Rosiglitazone; Thermodynamics; Thiazolidinediones

2010