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基于网络药理学和分子对接研究蒜氨酸激活自噬的多靶点机制。

Study on the multitarget mechanism of alliin activating autophagy based on network pharmacology and molecular docking.

机构信息

Jilin Agricultural Science and Technology University, Jilin, China.

出版信息

J Cell Mol Med. 2022 Nov;26(22):5590-5601. doi: 10.1111/jcmm.17573. Epub 2022 Oct 21.

Abstract

Due to the rapid development of bioinformatics, network pharmacology and molecular docking approaches have been successfully applied in the investigation of mechanisms of action. Here, we combined network pharmacology and molecular docking to predict the targets and reveal the molecular mechanism responsible for regulating autophagy by alliin. Based on the influence of alliin on autophagy, the targets of alliin were screened on the basis of different rules such as structural similarity by Pharmmapper, and genes associated with autophagy were collected from the GeneCards database. We focused on clarifying the biological processes and signalling pathways related to autophagy. Through the cytoHubba plug-in and a series of integrated bioinformatics analyses, the top nine hub nodes with higher degrees were obtained. And finally, through the LibDock included in Discovery Studio 2019, molecular docking method was adopted to declare the reliability of the interaction between alliin and hub targets. The results suggest that alliin-activated autophagy was possibly associated with pathways in cancer and the PI3K-AKT signalling pathway. Furthermore, the potential targets (AKT1, MAPK14, MAPK, HSPA8, EGFR, HSP90AA1, SRC HSPA1A and HSP90AB1) were swimmingly screened on the basis of this practical strategy. Molecular docking analysis indicates that alliin can bind with AKT1 and EGFR with good binding scores. This network pharmacology could be an invaluable strategy for the investigation of action mechanisms of alliin-activated autophagy. This study not only provides new and systematic insights into the underlying mechanism of alliin on autophagy, but also provides novel ideas for network approaches for autophagy-related research.

摘要

由于生物信息学的快速发展,网络药理学和分子对接方法已成功应用于作用机制的研究。在这里,我们结合网络药理学和分子对接来预测作用机制,并揭示蒜氨酸调节自噬的分子机制。基于蒜氨酸对自噬的影响,我们基于 Pharmmapper 的不同规则(如结构相似性)筛选蒜氨酸的靶点,并从 GeneCards 数据库中收集与自噬相关的基因。我们专注于阐明与自噬相关的生物学过程和信号通路。通过 cytoHubba 插件和一系列综合的生物信息学分析,获得了九个具有较高度数的顶级枢纽节点。最后,通过 Discovery Studio 2019 中包含的 LibDock,采用分子对接方法来声明蒜氨酸与枢纽靶点之间相互作用的可靠性。结果表明,蒜氨酸激活的自噬可能与癌症途径和 PI3K-AKT 信号通路有关。此外,根据这一实用策略,还成功筛选出潜在的靶标(AKT1、MAPK14、MAPK、HSPA8、EGFR、HSP90AA1、SRC HSPA1A 和 HSP90AB1)。分子对接分析表明,蒜氨酸可以与 AKT1 和 EGFR 结合,具有良好的结合评分。该网络药理学为研究蒜氨酸激活自噬的作用机制提供了一种非常有价值的策略。本研究不仅为蒜氨酸对自噬的作用机制提供了新的系统见解,也为自噬相关研究的网络方法提供了新的思路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ce1/9667524/6a15c612f5a3/JCMM-26-5590-g003.jpg

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