| Added by | Cavailles |
|---|---|
| Group name | EquipeVC |
| Item Type | Journal Article |
| Title | An Unexpected Mode Of Binding Defines BMS948 as A Full Retinoic Acid Receptor ? (RAR?, NR1B2) Selective Agonist |
| Creator | Nadendla et al. |
| Author | Eswarkumar Nadendla |
| Author | Catherine Teyssier |
| Author | Vanessa Delfosse |
| Author | Valérie Vivat |
| Author | Gunasekaran Krishnasamy |
| Author | Hinrich Gronemeyer |
| Author | William Bourguet |
| Author | Pierre Germain |
| Abstract | Retinoic acid is an important regulator of cell differentiation which plays major roles in embryonic development and tissue remodeling. The biological action of retinoic acid is mediated by three nuclear receptors denoted RAR?, ? and ?. Multiple studies support that RAR? possesses functional characteristics of a tumor suppressor and indeed, its expression is frequently lost in neoplastic tissues. However, it has been recently reported that RAR? could also play a role in mammary gland tumorigenesis, thus demonstrating the important but yet incompletely understood function of this receptor in cancer development. As a consequence, there is a great need for RAR?-selective agonists and antagonists as tools to facilitate the pharmacological analysis of this protein in vitro and in vivo as well as for potential therapeutic interventions. Here we provide experimental evidences that the novel synthetic retinoid BMS948 is an RAR?-selective ligand exhibiting a full transcriptional agonistic activity and activating RAR? as efficiently as the reference agonist TTNPB. In addition, we solved the crystal structures of the RAR? ligand-binding domain in complex with BMS948 and two related compounds, BMS641 and BMS411. These structures provided a rationale to explain how a single retinoid can be at the same time an RAR? antagonist and an RAR? full agonist, and revealed the structural basis of partial agonism. Finally, in addition to revealing that a flip by 180° of the amide linker, that usually confers RAR? selectivity, accounts for the RAR? selectivity of BMS948, the structural analysis uncovers guidelines for the rational design of RAR?-selective antagonists. |
| Publication | PloS One |
| Volume | 10 |
| Issue | 5 |
| Pages | e0123195 |
| Date | 2015 |
| Journal Abbr | PLoS ONE |
| Language | eng |
| DOI | 10.1371/journal.pone.0123195 |
| ISSN | 1932-6203 |
| Library Catalog | PubMed |
| Extra | PMID: 25933005 PMCID: PMC4416907 |
| Tags | Crystallography, X-Ray, HeLa Cells, Humans, Imidazoles, Ligands, Models, Molecular, original, Protein Binding, Protein Structure, Tertiary, Receptors, Retinoic Acid, Retinoic Acid Receptor alpha, Structure-Activity Relationship |
| Date Added | 2019/05/16 - 11:32:07 |
| Date Modified | 2019/05/16 - 11:36:39 |
| Notes and Attachments | PubMed entry (Attachment) Texte intégral (Attachment) |
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