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基于配体的虚拟筛选和分子动力学模拟发现鞘氨醇-1-磷酸受体调节剂作为潜在的几丁质酶3样蛋白1抑制剂

Discovery of Sphingosine-1-Phosphate Receptor Modulators as Potential CHI3L1 Inhibitors by Ligand-Based Virtual Screening and Molecular Dynamics Simulations.

作者信息

Aledavood Elnaz, Gil Carmen, Comabella Manuel, Martinez Ana

机构信息

Centro de Investigaciones Biologicas "Margarita Salas" (CIB-CSIC), Ramiro de Maeztu 9, Madrid 28040, Spain.

Centro de Investigación Biomédica en Red en Enfermedades Neurodegenerativas (CIBERNED), Instituto de Salud Carlos III, Melchor Fernández Almagro 3, Madrid 28029, Spain.

出版信息

ACS Omega. 2025 May 6;10(19):19992-20000. doi: 10.1021/acsomega.5c01968. eCollection 2025 May 20.

Abstract

Multiple sclerosis is characterized by central nervous system inflammation, demyelination, and neuronal degeneration. Current diagnostic and prognostic methods lack precision, necessitating biomarkers for personalized treatment strategies. Chitinase 3-like 1 (CHI3L1) has emerged as a potential prognostic marker, with elevated levels correlating with disease severity and relapse risk. Despite its therapeutic potential, few CHI3L1 inhibitors have been identified. Using ligand-based virtual screening and molecular dynamics simulations, Food and Drug Administration-approved drugs have been screened as CHI3L1 inhibitors with the final goals of being repurposed in MS and other inflammatory diseases, offering promising therapeutic approaches. This investigation suggests that sphingosine-1-phosphate receptor modulators such as fingolimod could be potential inhibitors for CHI3L1.

摘要

多发性硬化症的特征是中枢神经系统炎症、脱髓鞘和神经元变性。目前的诊断和预后方法缺乏精确性,因此需要生物标志物来制定个性化治疗策略。几丁质酶3样1(CHI3L1)已成为一种潜在的预后标志物,其水平升高与疾病严重程度和复发风险相关。尽管CHI3L1具有治疗潜力,但已鉴定出的CHI3L1抑制剂很少。通过基于配体的虚拟筛选和分子动力学模拟,已筛选出美国食品药品监督管理局批准的药物作为CHI3L1抑制剂,最终目标是将其重新用于治疗多发性硬化症和其他炎症性疾病,提供了有前景的治疗方法。这项研究表明,像芬戈莫德这样的鞘氨醇-1-磷酸受体调节剂可能是CHI3L1的潜在抑制剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff97/12096210/37584f89d804/ao5c01968_0001.jpg

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