Suppr超能文献

五环三萜类化合物抑制IKKβ介导的NF-κB信号通路激活:计算机模拟和体外实验证据

Pentacyclic Triterpenoids Inhibit IKKβ Mediated Activation of NF-κB Pathway: In Silico and In Vitro Evidences.

作者信息

Patil Kalpesh R, Mohapatra Purusottam, Patel Harun M, Goyal Sameer N, Ojha Shreesh, Kundu Chanakya N, Patil Chandragouda R

机构信息

Department of Pharmacology, H. R. Patel Institute of Pharmaceutical Education and Research, Shirpur, Dist- Dhule, Maharashtra, India.

Cancer Biology Laboratory, KIIT School of Biotechnology, KIIT University, Bhubaneswar, Odisha, India.

出版信息

PLoS One. 2015 May 4;10(5):e0125709. doi: 10.1371/journal.pone.0125709. eCollection 2015.

Abstract

Pentacyclic Triterpenoids (PTs) and their analogues as well as derivatives are emerging as important drug leads for various diseases. They act through a variety of mechanisms and a majority of them inhibit the nuclear factor kappa-beta (NF-κB) signaling pathway. In this study, we examined the effects of the naturally occurring PTs on IκB kinase-β (IKKβ), which has great scientific relevance in the NF-κB signaling pathway. On virtual screening, 109 PTs were screened through the PASS (prediction of activity spectra of substances) software for prediction of NF-κB inhibitory activity followed by docking on the NEMO/IKKβ association complex (PDB: 3BRV) and testing for compliance with the softened Lipinski's Rule of Five using Schrodinger (LLC, New York, USA). Out of the projected 45 druggable PTs, Corosolic Acid (CA), Asiatic Acid (AA) and Ursolic Acid (UA) were assayed for IKKβ kinase activity in the cell free medium. The UA exhibited a potent IKKβ inhibitory effect on the hotspot kinase assay with IC50 of 69 μM. Whereas, CA at 50 μM concentration markedly reduced the NF-κB luciferase activity and phospho-IKKβ protein expressions. The PTs tested, attenuated the expression of the NF-κB cascade proteins in the LPS-stimulated RAW 264.7 cells, prevented the phosphorylation of the IKKα/β and blocked the activation of the Interferon-gamma (IFN-γ). The results suggest that the IKKβ inhibition is the major mechanism of the PTs-induced NF-κB inhibition. PASS predictions along with in-silico docking against the NEMO/IKKβ can be successfully applied in the selection of the prospective NF-κB inhibitory downregulators of IKKβ phosphorylation.

摘要

五环三萜类化合物(PTs)及其类似物和衍生物正成为治疗各种疾病的重要药物先导物。它们通过多种机制发挥作用,其中大多数抑制核因子κB(NF-κB)信号通路。在本研究中,我们研究了天然存在的PTs对IκB激酶-β(IKKβ)的影响,IKKβ在NF-κB信号通路中具有重要的科学意义。通过虚拟筛选,利用PASS(物质活性谱预测)软件筛选了109种PTs以预测NF-κB抑制活性,随后对接NEMO/IKKβ关联复合物(PDB:3BRV),并使用Schrodinger(美国纽约LLC公司)测试其是否符合宽松的Lipinski五规则。在预计的45种可成药PTs中,对科罗索酸(CA)、积雪草苷(AA)和熊果酸(UA)在无细胞培养基中进行了IKKβ激酶活性测定。UA在热点激酶测定中对IKKβ表现出强效抑制作用,IC50为69μM。而50μM浓度的CA显著降低了NF-κB荧光素酶活性和磷酸化IKKβ蛋白表达。所测试的PTs减弱了LPS刺激的RAW 264.7细胞中NF-κB级联蛋白的表达,阻止了IKKα/β的磷酸化并阻断了干扰素-γ(IFN-γ)的激活。结果表明,IKKβ抑制是PTs诱导NF-κB抑制的主要机制。PASS预测以及针对NEMO/IKKβ的计算机模拟对接可成功应用于选择IKKβ磷酸化的潜在NF-κB抑制性下调剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e7a/4418667/ffec9a81720b/pone.0125709.g001.jpg

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