School of Chinese Medicine, Hunan University of Chinese Medicine, Changsha 410200, China.
Department of Biological Sciences, National University of Medical Sciences (NUMS), Rawalpindi 46000, Pakistan.
Molecules. 2023 Jun 21;28(13):4885. doi: 10.3390/molecules28134885.
IL-1β mediates inflammation and regulates immune responses, cell proliferation, and differentiation. Dysregulation of IL-1β is linked to inflammatory and autoimmune diseases. Elevated IL-1β levels are found in patients with severe COVID-19, indicating its excessive production may worsen the disease. Also, dry eye disease patients show high IL-1β levels in tears and conjunctival epithelium. Therefore, IL-1β signaling is a potential therapeutic targeting for COVID-19 and aforementioned diseases. No small-molecule IL-1β inhibitor is clinically approved despite efforts. Developing such inhibitors is highly desirable. Herein, a docking-based strategy was used to screen the TCM (Traditional Chinese Medicine) database to identify possible IL-1β inhibitors with desirable pharmacological characteristics by targeting the IL-1β/IL-1R interface. Primarily, the docking-based screening was performed by selecting the crucial residues of IL-1β interface to retrieve the potential compounds. Afterwards, the compounds were shortlisted on the basis of binding scores and significant interactions with the crucial residues of IL-1β. Further, to gain insights into the dynamic behavior of the protein-ligand interactions, MD simulations were performed. The analysis suggests that four selected compounds were stabilized in an IL-1β pocket, possibly blocking the formation of an IL-1β/IL-1R complex. This indicates their potential to interfere with the immune response, making them potential therapeutic agents to investigate further.
IL-1β 介导炎症反应,调节免疫应答、细胞增殖和分化。IL-1β 的失调与炎症和自身免疫性疾病有关。严重 COVID-19 患者的 IL-1β 水平升高,表明其过度产生可能使疾病恶化。此外,干眼症患者的泪液和结膜上皮中 IL-1β 水平较高。因此,IL-1β 信号通路是 COVID-19 和上述疾病的潜在治疗靶点。尽管进行了努力,但仍没有临床批准的小分子 IL-1β 抑制剂。开发这种抑制剂是非常可取的。在此,我们采用基于对接的策略筛选中药(TCM)数据库,通过靶向 IL-1β/IL-1R 界面,寻找具有理想药理特性的可能的 IL-1β 抑制剂。首先,通过选择 IL-1β 界面的关键残基进行基于对接的筛选,以检索潜在的化合物。然后,根据结合分数和与 IL-1β 关键残基的显著相互作用对化合物进行筛选。此外,为了深入了解蛋白质-配体相互作用的动态行为,我们进行了 MD 模拟。分析表明,四种选定的化合物在 IL-1β 口袋中稳定,可能阻止 IL-1β/IL-1R 复合物的形成。这表明它们有可能干扰免疫反应,使它们成为有潜力的治疗药物,值得进一步研究。