IIUM Repository

In silico study of the ErbB4 interactions with curcumin analogs

Azman, Putri Arsyadian and Abd Halim, Khairul Bariyyah (2015) In silico study of the ErbB4 interactions with curcumin analogs. In: 6th Regional Conference on Molecular Medicine (RCMM) in Conjunction with 2nd National Conference for Cancer Research 2015, 23rd-25th Oct. 2015, Sunway Putra Hotel, Kuala Lumpur. (Unpublished)

[img] PDF - Published Version
Restricted to Repository staff only

Download (150kB) | Request a copy

Abstract

Curcumin (diferuloylmethane) is generally found as the major compound in rhizomes of turmeric plants Curcuma longa Linaeusas. Curcumin has been shown to inhibit cancer growth by means of inhibiting ErBB family members (ErbB1, Erbb2, ErbB3 and ErbB4). This family receptors often targeted for development of cancer therapeutics. Previously, curcumin has also been shown to selectively inhibit EGFR or ErbB1 in in vitro, in vivo as well as in silico studies. However, its inhibitive effect on ErbB4 has not been elucidated. The present study evaluated the efficacy of natural curcumin and its analogs as ErbB4 inhibitors using computational approach namely molecular docking and molecular dynamics simulation. These approaches have been used to investigate the interactions between ErbB4 with curcumin analogs. Our molecular docking simulation showed that among five ligands that were docked at the active site cavity of ErbB4, ligand D docked with the lowest binding energy which was -7.29 kcal/mol. Ligand D which was the lowest energy complex obtained from docking experiment was then further investigated using molecular dynamics simulations. Ligand D were quite well oriented in the binding pocket throughout the 10 ns simulations. Molecular docking and molecular dynamics (MD) simulation studies showed that curcumin could be embedded into the hydrophobic pocket of ErbB4 and form stable hydrogen bonding interactions mainly with residue LYS-59. In conclusion, we have explored the binding mechanism of curcumin binding to ErbB4. This work could offer useful insight for designing novel analogs of curcumin as potential ErbB family inhibitors in the future.

Item Type: Conference or Workshop Item (Abstract)
Additional Information: 7228/48249
Uncontrolled Keywords: Silico study, ErbB4, curcumin
Subjects: R Medicine > R Medicine (General)
Kulliyyahs/Centres/Divisions/Institutes (Can select more than one option. Press CONTROL button): Kulliyyah of Science > Department of Biotechnology
Depositing User: Dr Khairul Bariyyah Abd Halim
Date Deposited: 28 Apr 2016 11:18
Last Modified: 28 Apr 2016 11:18
URI: http://irep.iium.edu.my/id/eprint/48249

Actions (login required)

View Item View Item

Downloads

Downloads per month over past year