Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC), 67400 Illkirch, France.
Institut National de La Santé et de La Recherche Médicale (INSERM), U1258, 67400 Illkirch, France.
J Med Chem. 2020 Sep 10;63(17):9457-9463. doi: 10.1021/acs.jmedchem.0c00656. Epub 2020 Aug 20.
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.
维生素 D 受体(VDR)拮抗剂阻止 VDR 激活功能螺旋 12 折叠成其活性构象,从而影响共激活因子的募集,并拮抗 1α,25-二羟维生素 D3 诱导的转录调节。在这里,我们报告了斑马鱼 VDR 配体结合域与 ZK168281 拮抗剂复合物的晶体结构,揭示了配体阻止了 VDR C 端区域的最佳折叠。这一干扰通过溶液中的氢氘交换质谱(HDX-MS)得到了证实。