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Structural Analysis of VDR Complex with ZK168281 Antagonist.

Anna Y BelorusovaSandra ChalhoubDaniela RovitoNatacha Rochel
Published in: Journal of medicinal chemistry (2020)
Vitamin D receptor (VDR) antagonists prevent the VDR activation function helix 12 from folding into its active conformation, thus affecting coactivator recruitment and antagonizing the transcriptional regulation induced by 1α,25-dihydroxyvitamin D3. Here, we report the crystal structure of the zebrafish VDR ligand-binding domain in complex with the ZK168281 antagonist, revealing that the ligand prevents optimal folding of the C-terminal region of VDR. This interference was confirmed by hydrogen-deuterium exchange mass spectrometry (HDX-MS) in solution.
Keyphrases
  • mass spectrometry
  • molecular dynamics simulations
  • single molecule
  • multiple sclerosis
  • ms ms
  • gas chromatography
  • dna binding
  • capillary electrophoresis
  • transcription factor