Molecular Docking and Dynamics Simulation Reveal Stable Binding of Tiliroside in the Colchicine Site of Tubulin

分子对接和动力学模拟揭示了Tiliroside与微管蛋白秋水仙碱结合位点的稳定结合。

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Abstract

BACKGROUND: The colchicine-binding site on tubulin is of particular interest for new drug development due to its role in microtubule destabilization and potential to overcome resistance to other agents. Tiliroside, a naturally occurring flavonoid glycoside, has demonstrated anticancer potential in vitro, but its interaction with tubulin has not been previously elucidated. OBJECTIVE: This study aimed to investigate the binding of tiliroside to the tubulin site of colchicine, in comparison with colchicine. METHODS: Molecular docking and molecular dynamics (MD) simulations were employed. Induced-fit docking predicted tiliroside binding, and redocking of colchicine was used to validate the docking protocol. MD simulations (100 ns) were conducted for both tubulin-tiliroside and tubulin-colchicine complexes. RESULTS: Induced-fit docking predicted that tiliroside binds strongly in the colchicine site, with more favorable scoring metrics than colchicine (Glide GScore -16.77 vs -10.25, and MMGBSA ΔG(bind) -50.46 vs -36.62 kcal/mol). Redocking of colchicine reproduced the binding pose (root-mean-square deviation (RMSD) ~0.6 Å). MD simulations further revealed that tiliroside forms a stable complex, remaining securely bound in the pocket. Tiliroside maintained multiple hydrogen bonds and hydrophobic contacts with tubulin, similar to or more persistent than those of colchicine. CONCLUSION: These results suggest that tiliroside can stably and snugly occupy the colchicine site of tubulin. In summary, our computational study provides structural and dynamic evidence that tiliroside is a high-affinity ligand for the colchicine site, supporting its potential as a lead compound for developing new tubulin-targeted anticancer agents.

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