A combined molecular docking and molecular dynamics simulation approach to probing the host–guest interactions of Ataluren with natural and modified cyclodextrins

ABSTRACT

The objective of this study was to apply molecular docking and molecular dynamics (MDs) simulation approaches to investigate the host–guest interactions between natural Cyclodextrins (CDs) (Alpha, Beta and Gamma Cyclodextrins) and some modified CDs (hydroxypropyl, sulfobutylether and randomly substituted methyl Beta Cyclodextrins) with Ataluren as a small molecule drug designed for diseases attributable to a nonsense mutation. Molecular docking results presented that randomly substituted methyl beta Cyclodextrin (RMBCD) has the highest binding affinity and Alpha Cyclodextrin (ACD) has the lowest binding affinity to Ataluren. According to the MDs simulation results, ACD and hydroxypropyl Cyclodextrin have not proper cavity for encapsulation of Ataluren. In contrast, Ataluren was totally included into the Beta Cyclodextrin (BCD), Gamma Cyclodextrin, sulfobutylether Beta Cyclodextrin (SBECD) and RMBCD due to appropriate interior capability. Moreover, MDs results showed that SBECD has the most conformational flexibility and BCD has the most conformational stability during simulation time. The results of this paper may open new paths to use this formulation for further researches in the delivery mechanism of hydrophobic pharmaceutical molecules.

KEYWORDS:

• Ataluren
• natural and modified cyclodextrins
• inclusion complex
• molecular docking
• molecular dynamics simulation

Acknowledgment

The authors would like to acknowledge the support of the Islamic Azad University (South Tehran Branch) and Pasteur Institute of Iran. The authors thank Dr Najme Fani for her technical assistance and controlling calculations. Also the authors appreciate Dr Isis G. Sarmiento for her scientific editing over the manuscript.

Disclosure statement

No potential conflict of interest was reported by the author(s).

Notes

1 Premature Termination Codon.