Computational exploration of natural product inhibitors against mutant Plasmodium falciparum DHFR through pharmacophore modeling, docking, and MD simulations

通过药效团建模、分子对接和分子动力学模拟,对天然产物抑制剂对抗突变型恶性疟原虫二氢叶酸还原酶(DHFR)进行计算探索

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Abstract

Drug-resistant Plasmodium falciparum has been on the rise, mainly due to point mutations in the pfDHFR or dihydrofolate reductase gene. This has heightened urgency to discover and develop new antimalarial drugs. This research utilized Pharmacophore Modeling, Virtual Screening, Molecular Docking and Molecular Dynamics Simulation techniques to identify potential pfDHFR inhibitors from virtual databases. Ligand-based pharmacophore hypothesis (H1) (r = 0.949, r(2) = 0.883) was formulated using a training set of 28 compounds that demonstrated pfDHFR inhibitory activity across four orders of magnitude. Additionally, a Structure-based Pharmacophore Hypothesis (P1) was derived from the ligand-binding site in the pfDHFR protein. The thoroughly validated hypotheses (H1 and P1) were then employed as 3D queries to screen compounds from the chemical database. These compounds were initially screened for drug-likeness and ADME/Tox properties before undergoing pharmacophore mapping. Pharmacophore mapping and docking analyses, followed by 200 ns molecular dynamics simulations using a mutant pfDHFR model, identified three promising lead candidates from the TCM database. The top compound, ZINC70454408, exhibited the highest H Bond energy of -14.204 kcal/mol and a predicted Ki of 0.04 µM, maintaining structural stability with an average RMSD of 2.1 Å throughout the simulation. Two additional compounds, ZINC04096650 and ZINC85631105, also exhibited strong binding energies (- 122.64 and - 118.92 kcal/mol, respectively) and low predicted Ki values (< 0.1 µM), with stable RMSD values ranging between 2.0 and 2.4 Å. These findings underscore ZINC70454408 as the most promising natural product-based pfDHFR inhibitor candidate and provide a compelling rationale for future experimental validation. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s40203-025-00533-z.

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