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

原肌球蛋白受体激酶B 受体酪氨酸激酶 对接(动物) trk受体 原肌球蛋白受体激酶A 药物发现 虚拟筛选 激酶 受体 药理学 化学 神经营养因子 神经营养素 生物 癌症研究 生物化学 医学 护理部
作者
Mohammed Ageeli Hakami,Bader S. Alotaibi,Ali Hazazi,Alaa Shafie,Ahad Amer Alsaiari,Amal Adnan Ashour,Farah Anjum
出处
期刊:Journal of Biomolecular Structure & Dynamics [Taylor & Francis]
卷期号:42 (6): 2965-2975 被引量:2
标识
DOI:10.1080/07391102.2023.2212786
摘要

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
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