Back to Search Start Over

Chromatin modification by olive phenolics: In silico molecular docking studies utilising the phenolic groups categorised in the OliveNetâ„¢ database against lysine specific demethylase enzymes.

Authors :
Pitsillou E
Liang J
Hung A
Karagiannis TC
Source :
Journal of molecular graphics & modelling [J Mol Graph Model] 2020 Jun; Vol. 97, pp. 107575. Date of Electronic Publication: 2020 Feb 26.
Publication Year :
2020

Abstract

Extra virgin olive oil is the principal source of dietary fat in the Mediterranean diet and is considered to have beneficial health effects. There is evidence to suggest that the phenolic compounds within Olea europaea have the ability to inhibit lysine-specific demethylase 1 (LSD1). This is an epigenetic enzyme that removes methyl groups from histone proteins and regulates gene transcription. Conversely, SET domain-containing protein 7 (SETD7) has opposing enzymatic activity and is a histone methyltransferase. Due to the involvement of these proteins in a number of pathological processes, including cancer and diabetes, further research needs to be conducted into the way in which they can be targeted. A large number of phenolic compounds (>200) have been identified in Olea europaea. To help expedite the discovery of promising lead compounds, in this study, in silico molecular docking methods were used to investigate the molecular binding properties of the phenolic compounds obtained from the OliveNetâ„¢ database to LSD1 and its variants, LSD2, and SETD7. Numerous Olea europaea phenolic compounds were predicted to bind to the epigenetic enzymes and several had stronger binding affinities than the LSD1 and SETD7 positive control inhibitors. The protein-ligand interactions of the phenolic compounds were also compared to known inhibitors and the molecular docking results suggest that the flavonoids, secoiridoids and glucosides may bind particularly strongly to the epigenetic regulators. Overall, several ligands were identified as lead compounds from this research and their potential inhibitory activity could be validated further in the laboratory.<br />Competing Interests: Declaration of competing interest Although no direct conflict of interest with respect to this article, the Epigenomic Medicine Program (TCK) is supported financially by McCord Research (Iowa, USA), which has commercial interests in nutraceuticals, some of which may have been discussed in this article. The remaining co-authors have no conflicts of interest.<br /> (Copyright © 2020 Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1873-4243
Volume :
97
Database :
MEDLINE
Journal :
Journal of molecular graphics & modelling
Publication Type :
Academic Journal
Accession number :
32126499
Full Text :
https://doi.org/10.1016/j.jmgm.2020.107575