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L.的表观基因组学营养见解:靶向DNA甲基转移酶和组蛋白脱乙酰酶的生物活性分子的计算分析

Epigenomics Nutritional Insights of L.: Computational Analysis of Bioactive Molecules Targeting DNA Methyltransferases and Histone Deacetylases.

作者信息

Piergentili Alessia, Saraceni Paolo Roberto, Demurtas Olivia Costantina, Benassi Barbara, Arcangeli Caterina

机构信息

Institute for Neuroscience and Medicine (INM-9), Forschungszentrum Jülich, Wilhelm-Johnen-Straße, 52428 Jülich, Germany.

Department of Neurology, University Hospital Aachen, RWTH Aachen, Pauwelsstraße 30, 52074 Aachen, Germany.

出版信息

Int J Mol Sci. 2025 Aug 5;26(15):7575. doi: 10.3390/ijms26157575.

Abstract

Saffron ( L.) contains bioactive compounds with potential health benefits, including modulation of protein function and gene expression. However, their ability to tune the epigenetic machine remains poorly understood. This study employs molecular docking (AutoDock Vina 1.4), dynamics simulations, and MM/PBSA calculations to investigate the interactions between four saffron-derived molecules-crocetin, beta-D-glucosyl trans-crocetin, picrocrocin and safranal-and four epigenetic enzymes-DNMT1, DNMT3a, HDAC2, and SIRT1. Our in silico screening identifies beta-D-glucosyl trans-crocetin, one of the saffron's crocins, as a potential DNMT1 inhibitor. Along with crocetin, it also shows the ability to inhibit HDAC2 and activate SIRT1. Picrocrocin displays a resveratrol-like ability to activate SIRT1. None of the saffron-derived compounds effectively bind or inhibit DNMT3a. Among the tested molecules, safranal shows no interaction with the selected epigenetic targets. These findings highlight saffron's nutriepigenomic potential and emphasize the need for functional validation within relevant in vitro and in vivo experimental methodologies.

摘要

藏红花(Crocus sativus L.)含有具有潜在健康益处的生物活性化合物,包括对蛋白质功能和基因表达的调节作用。然而,它们调节表观遗传机制的能力仍知之甚少。本研究采用分子对接(AutoDock Vina 1.4)、动力学模拟和MM/PBSA计算,来研究四种源自藏红花的分子——藏红花酸、β-D-葡萄糖基反式藏红花酸、苦藏花素和藏红花醛——与四种表观遗传酶——DNA甲基转移酶1(DNMT1)、DNA甲基转移酶3a(DNMT3a)、组蛋白去乙酰化酶2(HDAC2)和沉默调节蛋白1(SIRT1)——之间的相互作用。我们的计算机模拟筛选确定了藏红花的藏红花素之一β-D-葡萄糖基反式藏红花酸为一种潜在的DNMT1抑制剂。与藏红花酸一起,它还显示出抑制HDAC2和激活SIRT1的能力。苦藏花素表现出类似白藜芦醇激活SIRT1的能力。没有一种源自藏红花的化合物能有效结合或抑制DNMT3a。在所测试的分子中,藏红花醛与选定的表观遗传靶点没有相互作用。这些发现突出了藏红花营养表观基因组学的潜力,并强调了在相关体外和体内实验方法中进行功能验证的必要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3012/12347544/1b7f52abd4d3/ijms-26-07575-g003.jpg

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