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槲皮素对缺氧诱导因子(HIF)1α表达的调控:一项计算机模拟研究

The Regulation of Hypoxia Inducible Factor (HIF)1α Expression by Quercetin: an In Silico Study.

作者信息

Wahyuningsih Sri Puji Astuti, Dewi Firli Rahmah Primula, Hsan Amy Saik Yi, Lee Looi Mee, Lim Vuanghao, Aun Lionel In Lian, Ling Tau Chuan, Marviella Sephia Tiara

机构信息

Department of Biology, Faculty of Science and Technology, Universitas Airlangga, Surabaya, Indonesia.

Department of Pre-Clinical Sciences, Faculty of Medicine and Health Sciences, University Tunku Abdul Rahman, Malaysia.

出版信息

Acta Inform Med. 2022 Jun;30(2):96-99. doi: 10.5455/aim.2022.30.96-99.

Abstract

BACKGROUND

Cancer disease is a growing health problem in developing and developed countries. Hypoxia-inducible factor-1a (HIF1α) is a transcription factor responsible for expressing several proteins involved in angiogenesis. Quercetin can suppress HIF1α expression due to the inhibition of protein synthesis. However, to date, the study exploring the potential of quercetin in repressing HIF1α through its degradation mechanism has never been done. An in silico study is needed as a preliminary study to understand the mechanism underlining this possibility.

OBJECTIVE

This study aimed to investigate the potential of quercetin in regulating HIF1α expression through the ubiquitin degradation pathway by in silico study.

METHODS

This study was performed by in silico analysis, including biological activity prediction, 3D protein structure collection, protein-ligand and protein-protein docking, and the visualization of the docking results.

RESULTS

The probability activity (Pa) score of quercetin as an HIF1α expression inhibitor was 0.969. In the absence of quercetin, the center-weighted score of HIF1α - pVHL, HIF1α - FIH, and HIF1α - PHD2 was -699.4 kJ/mol, -846.0 kJ/mol, and -650.5 kJ/mol, respectively. In the presence of quercetin, the weighted score of HIF1α - pVHL, HIF1α - FIH, and HIF1α - PHD2 was reduced to -728.1 kJ/mol, -854.2 kJ/mol, and -650.5 kJ/mol, respectively.

CONCLUSION

Quercetin could directly promote HIF1α and pVHL interaction, thus increasing the degradation of HIF1α by ubiquitin-dependent pathway.

摘要

背景

癌症疾病在发展中国家和发达国家都是日益严重的健康问题。缺氧诱导因子-1α(HIF1α)是一种转录因子,负责表达多种参与血管生成的蛋白质。槲皮素可通过抑制蛋白质合成来抑制HIF1α的表达。然而,迄今为止,尚未开展过探索槲皮素通过其降解机制抑制HIF1α潜力的研究。需要进行一项计算机模拟研究作为初步研究,以了解这种可能性背后的机制。

目的

本研究旨在通过计算机模拟研究探讨槲皮素通过泛素降解途径调节HIF1α表达的潜力。

方法

本研究通过计算机模拟分析进行,包括生物活性预测、三维蛋白质结构收集、蛋白质-配体和蛋白质-蛋白质对接以及对接结果的可视化。

结果

槲皮素作为HIF1α表达抑制剂的概率活性(Pa)评分为0.969。在不存在槲皮素的情况下,HIF1α-pVHL、HIF1α-FIH和HIF1α-PHD2的中心加权分数分别为-699.4 kJ/mol、-846.0 kJ/mol和-650.5 kJ/mol。在存在槲皮素的情况下,HIF1α-pVHL、HIF1α-FIH和HIF1α-PHD2的加权分数分别降至-728.1 kJ/mol、-854.2 kJ/mol和-650.5 kJ/mol。

结论

槲皮素可直接促进HIF1α与pVHL的相互作用,从而增加泛素依赖性途径对HIF1α的降解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b9e7/9233451/416db0392631/AIM-30-96-g001.jpg

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