Harnessing machine learning for efficient large-scale interatomic potential for sildenafil and pharmaceuticals containing H, C, N, O, and S

Abstract

In this study a cutting-edge approach to producing accurate and computationally efficient interatomic potentials using machine learning algorithms is presented. Specifically, the study focuses on the application of Allegro, a novel machine learning algorithm, running on high-performance GPUs for training potentials. The choice of training parameters plays a pivotal role in the quality of the potential functions. To enable this methodology, the “Solvated Protein Fragments” dataset, containing nearly 2.7 million Density Functional Theory (DFT) calculations for many-body intermolecular interactions involving protein fragments and water molecules, encompassing H, C, N, O, and S elements, is considered as the training dataset. The project optimizes computational efficiency by reducing the initial dataset size according to the intended application. To assess the efficacy of the approach, the sildenafil citrate, iso-sildenafil, aspirin, ibuprofen, mebendazole and urea, representing all five relevant elements, serve as the test bed. The results of the Allegro-trained potentials demonstrate outstanding performance, benefiting from the combination of an appropriate training dataset and parameter selection. This notably enhanced computational efficiency when compared to the computationally intensive DFT method aided by GPU acceleration. Validation of the produced interatomic potentials is achieved through Allegro's own evaluation mechanism, yielding exceptional accuracy. Further verification is carried out through LAMMPS molecular dynamics simulations. Structural optimization by energy minimization and NPT Molecular Dynamics simulations are performed for each potential, assessing relaxation processes and energy reduction. Additional structures, including urea, ammonia, uracil, oxalic acid, and acetic acid, are tested, highlighting the potential's versatility in describing systems containing the aforementioned elements. Visualization of the results confirms the scientific accuracy of each structure's relaxation. The findings of this study demonstrate strong scaling and the potential for applications in pharmaceutical research, allowing the exploration of larger molecular structures not previously amenable to computational analysis at this level of accuracy The success of the machine learning approach underscores its potential to revolutionize computational solid-state physics.