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鉴定靶向 IL-1β/IL-1R 蛋白-蛋白界面的天然产物抑制剂。

Identification of Natural Product-Based Inhibitors Targeting IL-1β/IL-1R Protein-Protein Interface.

机构信息

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.

出版信息

Molecules. 2023 Jun 21;28(13):4885. doi: 10.3390/molecules28134885.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/797d/10343601/fedaa2f74457/molecules-28-04885-g001.jpg

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