HEIWA: Hybrid Explicit-Implicit Water Attention Affects Force Field Accuracy in Structure-Based Protein Language Model ESM3
Related Experiment Video
Updated: Nov 10, 2026

Modeling Ligands into Maps Derived from Electron Cryomicroscopy
Published on: July 19, 2024
Ngai Hei Ernest Ho1, Chao Tung Yang2,3,4, I-Son Ng1
1Department of Chemical Engineering, National Cheng Kung University, Tainan701, Taiwan.
Abstract:
Protein language models have achieved remarkable success in structure prediction and de novo design. However, their understanding of physical interactions remains limited. For structure-based models, we hypothesize that this limitation stems from the absence of explicit solvent modeling: water mediates hydrogen bonding, hydrophobic burial, and electrostatic interactions that govern protein thermodynamics and kinetics, yet current structure-based models treat proteins as if they exist in a vacuum. Using thermophilic protein classification as a proxy task for force-field awareness, per-residue logit mis-correlated with H-bonds as a destabilizing attribute and exhibits significant solvent-accessible surface area (SASA)-dependent error, despite high overall classification accuracy. These artifacts point to the water-protein interface as a source of systematic bias. To address this, we propose HEIWA (HybridExplicit-Implicit Water Attention), a novel attention module that injects solvent-mediated force-field information into static ESM3 residue embeddings via an all-query-to-all-key water-residue attention. Biophysics-guided model selection identifies configurations whose residue-level outputs are more consistent with the RMSF benchmark and selected biophysical attributes, while classification performance remains broadly comparable to the baseline. By forcing the model to predict the protein thermophilicity from the contributions of individual residues, HEIWA learns biophysical patterns that can be extended to SUPFAM absent from the training data set. HEIWA also largely preserves the embedding structure of ESM3. Molecular dynamics simulations show improved kinetic stability under thermophilic conditions, suggesting the potential to generate structures with greater kinetic stability. To our knowledge, this is the first study to incorporate explicit solvent encoding into a residue-resolution protein language model.
Related Concept Videos
Chemical Shift: Internal References and Solvent Effects
The internal reference compound generally used in NMR spectroscopy is tetramethylsilane (TMS). TMS is preferred because it is chemically inert, soluble in NMR solvents, and easily removable. Also, the highly shielded methyl protons in TMS yield an intense...
Noncovalent Attractions in Biomolecules
Four types of noncovalent interactions are hydrogen bonds, van der Waals forces, ionic bonds, and hydrophobic interactions.
Hydrogen bonding results from the electrostatic attraction of a hydrogen atom covalently bonded to a strong-electronegative atom like oxygen,...
Molecular Models
Globular and Fibrous Proteins
Globular proteins are also known as spheroproteins and typically are approximately round in shape. They contain a mix of amino acid types and contain differing sequences in their primary structures. Globular proteins have many different functions, such as enzymes, cellular messengers, and molecular transporters. These roles often require the proteins to be...

