Crystal structures of hereditary vitamin D-resistant rickets-associated vitamin D receptor mutants R270l and W282R bound to 1,25-dihydroxyvitamin D 3 and synthetic ligands

Makoto Nakabayashi, Yoshito Tsukahara, Yukiko Iwasaki-Miyamoto, Mika Mihori-Shimazaki, Sachiko Yamada, Satomi Inaba, Masayuki Oda, Masato Shimizu, Makoto Makishima, Hiroaki Tokiwa, Teikichi Ikura, Nobutoshi Ito

Research output: Contribution to journalArticlepeer-review

17 Citations (Scopus)

Abstract

The vitamin D receptor (VDR), a member of the nuclear receptor superfamily, functions as a ligand-dependent transcription factor for various genes. Hereditary vitamin D-resistant rickets (HVDRR), an autosomal recessive disease, is caused by mutations in the VDR. In particular, the missense mutations R274L and W286R in the ligand-binding domain of the VDR can severely reduce or even eliminate natural hormone responsiveness. Here, we report a crystal structure analysis of the R270L and W282R mutants of rat VDR (human R274L and W286R, respectively) in complex with the natural hormone and synthetic ligands. We also studied the folding properties of the mutant proteins by using circular dichroism spectra. Our study indicates that these mutations result in only local structural modifications. We discuss why these mutations disrupt the VDR function and provide clues to develop effective ligands for the treatment of HVDRR.

Original languageEnglish
Pages (from-to)6745-6760
Number of pages16
JournalJournal of medicinal chemistry
Volume56
Issue number17
DOIs
Publication statusPublished - Sep 12 2013

ASJC Scopus subject areas

  • Molecular Medicine
  • Drug Discovery

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