Evidence map›Paper›PMID 41542157›Full record

ArticleArXiv2026

Knowledge Distillation of a Protein Language Model Yields a Foundational Implicit Solvent Model.

Justin Airas, Bin Zhang

Abstract readPreprint
In one paragraph

Article in ArXiv, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors.

Justin AirasDepartment of Chemistry, Massachusetts Institute of Technology, Cambridge, MA, USA.
Bin ZhangDepartment of Chemistry, Massachusetts Institute of Technology, Cambridge, MA, USA.

Funding

Probing and Perturbing Transcriptional Condensates with Multiscale Modeling and Deep LearningR35GM133580 · NIGMS · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI Bin Zhang · 2019 to 2026
$3.1M
NIGMS NIH HHS R35 GM133580
6 · The paper itself

Abstract

Implicit solvent models (ISMs) promise to deliver the accuracy of explicit solvent simulations at a fraction of the computational cost. However, despite decades of development, their accuracy has remained insufficient for many critical applications, particularly for simulating protein folding and the behavior of intrinsically disordered proteins. Developing a transferable, data-driven ISM that overcomes the limitations of traditional analytical formulas remains a central challenge in computational chemistry. Here we address this challenge by introducing a novel strategy that distills the evolutionary information learned by a protein language model, ESM3, into a computationally efficient graph neural network (GNN). We show that this GNN potential, trained on effective energies from ESM3, is robust enough to drive stable, long-timescale molecular dynamics simulations. When combined with a standard electrostatics term, our hybrid model accurately reproduces protein folding free-energy landscapes and predicts the structural ensembles of intrinsically disordered proteins. This approach yields a single, unified model that is transferable across both folded and disordered protein states, resolving a long-standing limitation of conventional ISMs. By successfully distilling evolutionary knowledge into a physical potential, our work delivers a foundational implicit solvent model poised to accelerate the development of predictive, large-scale simulation tools.

Identifiers

PMID41542157
PMCPMC12803332

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.