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通过虚拟筛选和实验验证鉴定潜在的 TLR7 拮抗剂。

Identification of the potential TLR7 antagonists by virtual screening and experimental validation.

机构信息

Department of Dermatology, Second Xiangya Hospital, Central South University, Hunan Key Laboratory of Medical Epigenomics, Changsha, Hunan, China.

Department of Anesthesiology, Second Xiangya Hospital, Central South University, Changsha, Hunan, China.

出版信息

Mol Divers. 2024 Jun;28(3):1335-1346. doi: 10.1007/s11030-023-10660-4. Epub 2023 May 23.

Abstract

Toll-like receptor 7 (TLR7) is highly expressed in dendritic cells (DCs) and B cells, and its aberrant activation can promote disease progression in systemic lupus erythematosus (SLE). We utilized structure-based virtual screening and experimental validation to screen natural products from TargetMol for potential TLR7 antagonists. Our results of molecular docking and molecular dynamics simulation showed that Mogroside V (MV) strongly interacted with TLR7, with stable open-TLR7-MV and close-TLR7-MV complexes. Furthermore, in vitro experiments demonstrated that MV significantly inhibited B cell differentiation in a concentration-dependent manner. In addition to TLR7, we also revealed a strong interaction of MV with all TLRs, including TLR4. The above results suggested that MV might be a potential TLR7 antagonist deserving of further study.

摘要

Toll-like receptor 7 (TLR7) 在树突状细胞 (DCs) 和 B 细胞中高度表达,其异常激活可促进系统性红斑狼疮 (SLE) 的疾病进展。我们利用基于结构的虚拟筛选和实验验证,从 TargetMol 筛选天然产物,寻找潜在的 TLR7 拮抗剂。分子对接和分子动力学模拟的结果表明,罗汉果苷 V (MV) 与 TLR7 强烈相互作用,形成稳定的开放-TLR7-MV 和关闭-TLR7-MV 复合物。此外,体外实验表明,MV 以浓度依赖的方式显著抑制 B 细胞分化。除了 TLR7 之外,我们还发现 MV 与包括 TLR4 在内的所有 TLR 都有很强的相互作用。上述结果表明,MV 可能是一种有潜力的 TLR7 拮抗剂,值得进一步研究。

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