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Machine-learned molecular mechanics force fields from large-scale quantum chemical data
- Takaba, Kenichiro;
- Friedman, Anika J;
- Cavender, Chapin E;
- Behara, Pavan Kumar;
- Pulido, Iván;
- Henry, Michael M;
- MacDermott-Opeskin, Hugo;
- Iacovella, Christopher R;
- Nagle, Arnav M;
- Payne, Alexander Matthew;
- Shirts, Michael R;
- Mobley, David L;
- Chodera, John D;
- Wang, Yuanqing
Published Web Location
https://doi.org/10.1039/d4sc00690aAbstract
The development of reliable and extensible molecular mechanics (MM) force fields-fast, empirical models characterizing the potential energy surface of molecular systems-is indispensable for biomolecular simulation and computer-aided drug design. Here, we introduce a generalized and extensible machine-learned MM force field, espaloma-0.3, and an end-to-end differentiable framework using graph neural networks to overcome the limitations of traditional rule-based methods. Trained in a single GPU-day to fit a large and diverse quantum chemical dataset of over 1.1 M energy and force calculations, espaloma-0.3 reproduces quantum chemical energetic properties of chemical domains highly relevant to drug discovery, including small molecules, peptides, and nucleic acids. Moreover, this force field maintains the quantum chemical energy-minimized geometries of small molecules and preserves the condensed phase properties of peptides and folded proteins, self-consistently parametrizing proteins and ligands to produce stable simulations leading to highly accurate predictions of binding free energies. This methodology demonstrates significant promise as a path forward for systematically building more accurate force fields that are easily extensible to new chemical domains of interest.
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