Volume 11, Issue 3 (2020)                   JMBS 2020, 11(3): 59-69 | Back to browse issues page

XML Persian Abstract Print

Download citation:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:

abyar A, Bamdadi A, Behjatmanes A. Full Potential Study and Molecular Docking Interaction of Anticancer Drugs with Au Nanoparticle. JMBS 2020; 11 (3) :59-69
URL: http://biot.modares.ac.ir/article-22-41641-en.html
1- Ardakan University, ardakan-yazd , f.abyar@ardakan.ac.ir
2- Department of Chemistry, Payame Noor University, Tehran, Iran., ardakan-yazd
Abstract:   (3860 Views)
In the present study, the structure of three common anticancer drugs including 6-thioguanine (6-TG), hydroxyurea (NH) and busulfan were optimized using quantum computational and obtained minimum energy for them. Also, optimization structure of gold nanoparticle was investigated by density functional theory (DFT). Finally, the binding energy of Au nanoparticle was calculated with the optimized structures of drugs. All different sites of drugs that can be interacted with nanoparticle were considered and the most stable structure was chosen for further study. These calculations were performed using FHI-aims which is a software package based on DFT. The bond length and the best interaction energy were reported in this work. To better investigation of the location of the interaction, the type of orbitals involved in the interaction and their shapes are shown. Gap energy analysis showed that the lowest energy was related to the complex of gold nanoparticle with 6-thioguanine, which confirms the chemical stability of this drug with nanoparticle. Investigations showed that the binding energy of gold nanoparticle with drugs is busulfan > hydroxyurea> 6-thioguanine so busulfan has more affinity to bind with gold nanoparticle.
Au nanoparticle as an anticancer drug deliver was studied with the molecular docking calculations. The human albumin serum (HSA) binding with three anticancer drugs was docked individually with Hex 8 software and their active sites of interaction were shown as well as.  Finally, the binding energies and types of interactions such as electrostatic, van der Waals and hydrogen bonds between HSA and Au@ drugs were presented, clearly.
Full-Text [PDF 1959 kb]   (2131 Downloads)    
Article Type: Original Research | Subject: Bioinformatics
Received: 2020/03/27 | Accepted: 2020/08/12 | Published: 2020/10/2

Add your comments about this article : Your username or Email:

Send email to the article author

Rights and permissions
Creative Commons License This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.