The Transferable Water Implicit Network (TWIN) is introduced, an implicit water MLP parametrized entirely by an Equivariant Graph Neural Network and trained solely on ab initio and experimental labels, consistently outperforming previous machine-learning-based implicit solvent or coarse-grained models.
Abstract
Machine learning interatomic potentials (MLPs) have revolutionized atomistic modeling, offering the potential to replace traditional methods like Density Functional Theory (DFT). However, inference time of MLPs is orders of magnitude slower than that of classical force fields, hindering real-world applications for biomolecular systems that require timescales of microseconds and beyond. Implicit solvent MLPs can address this issue, but are faced with data challenges associated with coarse-grained modeling. Consequently, previous approaches relied on empirical force field data, thereby inherently limiting the MLP's accuracy. Here, we introduce the Transferable Water Implicit Network (TWIN), an implicit water MLP parametrized entirely by an Equivariant Graph Neural Network and trained solely on ab initio and experimental labels. We demonstrate TWIN's transferability across drug-like molecules, peptides, and proteins, achieving excellent results on ab initio and experimental crystallographic and NMR benchmarks, consistently outperforming previous machine-learning-based implicit solvent or coarse-grained models. Furthermore, TWIN closely matches DFT-based explicit solvent MLPs while providing a two-order-of-magnitude faster timestep evaluation, paving the way for efficient ab initio-level modeling of biomolecular systems in aqueous environments.
DensIP is introduced, a physics-based model of intermolecular interactions that uses machine-learned electron densities and only four universal parameters that outperforms state-of-the-art general-purpose MLFFs for long-range interactions and can be applied to molecules as large as drug ligands.
Dahvyd Wing, Mihail Bogojeski, Szabolcs Góger et al.· 1 citation
Training a machine learning interatomic potential capable of probing the properties of aqueous methanol mixtures at the DFT level using the SCAN functional indicates that SCAN provides an accurate description of methanol–water mixtures, making it a reliable choice for investigating the reactive dynamics in such systems...
Sanghyun J. Park, A. Selloni· Journal of Physical Chemistr...· 0 citations
By identifying AIM methods that result in conformationally stable and transferable atomic properties, this study aims to improve IDP modelling and guide the development of more accurate force fields for biologically relevant systems.
While machine-learning interatomic potentials (MLIPs) have successfully learned potential energy surfaces (PES) and atomic forces, many practical applications, such as vibrational analysis and transition state search, rely heavily on the PES Hessian. Yet standard MLIPs are trained on energy and forces alone, and existi...
This work introduces implicit machine learning force fields, which replace explicit stacks of neural network layers with self-consistent fixed-point equations, and demonstrates this across three major classes of graph neural networks: invariant, equivariant Cartesian tensor, and SO(3)-equivariant spherical-tensor archi...
J. Maeß, Leon Werner, J. Frank et al.· arXiv.org· 0 citations
This study presents a method to derive optimized CV from transition state region (TS) via an interpretable machine learning (ML) model, Elastic Net, which greatly accelerate ligand binding-unbinding transitions and achieves rapid free energy surface (FES) convergence across diverse systems.
Saikat Dhibar, Biman Jana· bioRxiv· 1 citation
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