Molecular Dynamics Simulations to Investigate the Binding Mode of the Natural Product Liphagal with Phosphoinositide 3-Kinase α

作者：Gao, Yanjuan; Ma, Ying; Yang, Guangde; Li, Yiping^*

来源：Molecules, 2016, 21(7): 857.

DOI：10.3390/molecules21070857

• molecular dynamics simulation
• liphagal
• phosphatidylinositol 3-kinase
• binding mode
• anti-tumor

Phosphatidylinositol 3-kinase (PI3K) is an attractive target for anticancer drug design. Liphagal, isolated from the marine sponge Aka coralliphaga, possesses the special liphagane meroterpenoid carbon skeleton and has been demonstrated as a PI3K inhibitor. Molecular docking and molecular dynamics simulations were performed to explore the dynamic behaviors of PI3K binding with liphagal, and free energy calculations and energy decomposition analysis were carried out by use of molecular mechanics/Poisson-Boltzmann (generalized Born) surface area (MM/PB(GB)SA) methods. The results reveal that the heteroatom rich aromatic D-ring of liphagal extends towards the polar region of the binding site, and the D-ring 15-hydroxyl and 16-hydroxyl form three hydrogen bonds with Asp810 and Tyr836. The cyclohexyl A-ring projects up into the upper pocket of the lipophilic region, and the hydrophobic/van der Waals interactions with the residues Met772, Trp780, Ile800, Ile848, Val850, Met922, Phe930, Ile932 could be the key interactions for the affinity of liphagal to PI3K. Thus, a new strategy for the rational design of more potent analogs of liphagal against PI3K is provided. Our proposed PI3K/liphagal binding mode would be beneficial for the discovery of new active analogs of liphagal against PI3K alpha.

• 出版日期2016-7
• 单位西安交通大学