School of Biological Sciences, Nanyang Technological University, 60 Nanyang Drive, 637551, Singapore.
School of Biological Sciences, Nanyang Technological University, 60 Nanyang Drive, 637551, Singapore; College of Pharmacy, CHA University, 120 Haeryong-ro, Pocheon-si, Gyeonggi-do, 11160, Republic of Korea; CHA Advanced Research Institute, 335 Pangyo-ro, Bundang-gu, Seongnam-si, 13488, Republic of Korea.
Eur J Med Chem. 2023 Dec 5;261:115869. doi: 10.1016/j.ejmech.2023.115869. Epub 2023 Oct 11.
Nuclear receptors (NRs) are ligand-induced transcriptional factors implicated in several physiological pathways. Naïve ligands bind to their cognate receptors and modulate gene expression as agonists or antagonists. It has been observed that some ligands bind via covalent bonding with the NR Ligand Binding Domain (LBD) residues. While many such instances have been known since the 1980s, a consolidated account of these ligands and their interactions with NR-LBD is yet to be documented. To negate this, we have culled out the human NR-LBDs that form a covalent attachment with ligands. According to the study, 16 of the 48 human NRs have been targeted by covalent ligands. It was found that conserved cysteines prone to covalent attachment are predominantly located in NR-LBD helices 3 and 11. These conserved cysteines are also observed in many of the remaining NRs, which can be probed for their reactivity. Thus, the structural insights into NR-LBD interactions with covalent ligands presented here would aid drug discovery efforts targeting NRs.
核受体 (NRs) 是配体诱导的转录因子,参与多种生理途径。天然配体与同源受体结合,并作为激动剂或拮抗剂调节基因表达。已经观察到一些配体通过与核受体配体结合域 (LBD) 残基的共价键结合。虽然自 20 世纪 80 年代以来已经知道了许多这样的实例,但尚未记录这些配体及其与 NR-LBD 的相互作用的综合描述。为了消除这种情况,我们已经筛选出与配体形成共价键的人类 NR-LBD。根据这项研究,48 个人类 NR 中有 16 个被共价配体靶向。研究发现,易于发生共价结合的保守半胱氨酸主要位于 NR-LBD 螺旋 3 和 11 中。这些保守的半胱氨酸也存在于许多其他的 NR 中,可以探测它们的反应性。因此,这里提出的关于 NR-LBD 与共价配体相互作用的结构见解将有助于针对 NR 的药物发现工作。