Dual conformation of the ligand induces the partial agonistic activity of retinoid X receptor α (RXRα). Issue 2 (21st December 2018)

• Record Type: Journal Article
• Authors: Miyashita, Yurina; Numoto, Nobutaka; Arulmozhiraja, Sundaram; Nakano, Shogo; Matsuo, Naoya; Shimizu, Kanade; Shibahara, Osamu; Fujihara, Michiko; Kakuta, Hiroki; Ito, Sohei; Ikura, Teikichi; Ito, Nobutoshi; Tokiwa, Hiroaki
• Is Part Of: FEBS letters. Volume 593:Issue 2(2019)
• Page Start: 242
• Page End: 250
• Publication Date: 2018-12-21
• Subjects: biochemical analysis -- crystal structure -- fragment molecular orbital theory -- molecular dynamics simulations -- partial agonist -- RXRα; Biochemistry -- Periodicals; Biophysics -- Periodicals; Molecular biology -- Periodicals; Biochimie -- Périodiques; Biochemistry; Biophysics; Molecular biology; Periodicals; 572.05
• DOI: 10.1002/1873-3468.13301
• Languages: English
• ISSNs: 0014-5793

Abstract

Abstract : 1‐[(3, 5, 5, 8, 8‐pentamethyl‐5, 6, 7, 8‐tetrahydronaphthalen‐2‐yl)amino]benzotriazole‐5‐carboxylic acid (CBt‐PMN), a partial agonist of retinoid X receptor (RXR), has attracted attention due to its potential to treat type 2 diabetes and central nervous system diseases with reduced adverse effects of existing full agonists. Herein, we report the crystal structure of CBt‐PMN‐bound ligand‐binding domain of human RXRα (hRXRα) and its biochemical characterization. Interestingly, the structure is a tetramer in nature, in which CBt‐PMNs are clearly found binding in two different conformations. The dynamics of the hRXRα/CBt‐PMN complex examined using molecular dynamics simulations suggest that the flexibility of the AF‐2 interface depends on the conformation of the ligand. These facts reveal that the dual conformation of CBt‐PMN in the complex is probably the reason behind its partial agonistic activity. Abstract :