Suppr超能文献

鉴定靶向中枢神经系统相关疾病和癌症的原肌球蛋白受体激酶 B 的潜在抑制剂。

Identification of potential inhibitors of tropomyosin receptor kinase B targeting CNS-related disorders and cancers.

机构信息

Department of Clinical Laboratory Sciences, College of Applied Medical Sciences, Al-Quwayiyah, Shaqra University, Riyadh, Saudi Arabia.

Department of Pathology and Laboratory Medicine, Security Forces Hospital Program, Riyadh, Kingdom of Saudi Arabia.

出版信息

J Biomol Struct Dyn. 2024 Apr;42(6):2965-2975. doi: 10.1080/07391102.2023.2212786. Epub 2023 May 15.

Abstract

Tropomyosin receptor kinase B (TrkB), also known as neurotrophic tyrosine kinase receptor type 2 (NTRK2), is a protein that belongs to the family of receptor tyrosine kinases (RTKs). NTRK2 plays a crucial role in regulating the development and maturation of the central nervous system (CNS) and peripheral nervous system (PNS). Elevated TrkB expression levels observed in different pathological conditions make it a potential target for therapeutic interventions against neurological disorders, including depression, anxiety, Alzheimer's disease, Parkinson's disease, and certain types of cancer. Targeting TrkB using small molecule inhibitors is a promising strategy for the treatment of a variety of neurological disorders. In this research, a systematic virtual screening was carried out on phytoconstituents found in the IMPPAT library to identify compounds potentially inhibiting TrkB. The retrieved compounds from the IMPPAT library were first filtered using Lipinski's rule of five. The compounds were then sorted based on their docking score and ligand efficiency. In addition, PAINS, ADMET, and PASS evaluations were carried out for selecting drug-like compounds. Finally, in interaction analysis, we found two phytoconstituents, Wedelolactone and 3,8-dihydroxy-1-methylanthraquinone-2-carboxylic acid (DMCA), which possessed considerable docking scores and specificity on the TrkB ATP-binding pocket. The selected compounds were further assessed employing molecular dynamics (MD) simulations and essential dynamics. The results revealed that the elucidated compounds bind well with the TrkB binding pocket and lead to fewer conformations fluctuations. This study highlighted using phytoconstituents, Wedelolactone and DMCA as starting leads in developing novel TrkB inhibitors.Communicated by Ramaswamy H. Sarma.

摘要

原肌球蛋白受体激酶 B(TrkB),也称为神经营养酪氨酸激酶受体 2(NTRK2),是一种属于受体酪氨酸激酶(RTKs)家族的蛋白质。NTRK2 在调节中枢神经系统(CNS)和周围神经系统(PNS)的发育和成熟中起着至关重要的作用。在不同的病理条件下观察到的 TrkB 表达水平升高使其成为针对包括抑郁症、焦虑症、阿尔茨海默病、帕金森病和某些类型的癌症在内的神经障碍的治疗干预的潜在靶标。使用小分子抑制剂靶向 TrkB 是治疗各种神经障碍的有前途的策略。在这项研究中,对 IMPPAT 库中发现的植物成分进行了系统的虚拟筛选,以鉴定潜在抑制 TrkB 的化合物。从 IMPPAT 库中检索到的化合物首先使用 Lipinski 的五规则进行过滤。然后根据对接得分和配体效率对化合物进行排序。此外,还进行了 PAINS、ADMET 和 PASS 评估,以选择类药性化合物。最后,在相互作用分析中,我们发现了两种植物成分,即卫矛内酯和 3,8-二羟基-1-甲基蒽醌-2-羧酸(DMCA),它们在 TrkB ATP 结合口袋上具有相当大的对接得分和特异性。选择的化合物进一步通过分子动力学(MD)模拟和基本动力学进行评估。结果表明,阐明的化合物与 TrkB 结合口袋结合良好,并导致构象波动减少。这项研究强调了使用植物成分卫矛内酯和 DMCA 作为开发新型 TrkB 抑制剂的起始先导。由 Ramaswamy H. Sarma 传达。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验