Evidence map›Paper›PMID 39464109›Full record

ArticlebioRxiv : the preprint server for biology2025

Learning Biophysical Dynamics with Protein Language Models.

Chao Hou, Haiqing Zhao, Yufeng Shen

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. 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

3 authors.

Chao HouDepartment of Systems Biology, Columbia University Irving Medical Center, New York, NY 10032.ORCID 0000-0003-4806-7637
Haiqing ZhaoDepartment of Biochemistry and Molecular Biology, University of Texas Medical Branch, Galveston, TX 77555.
Yufeng ShenDepartment of Systems Biology, Columbia University Irving Medical Center, New York, NY 10032.ORCID 0000-0002-1299-5979

Funding

Computational methods to interpret genomic variation and integrate functional genomics data in genetic analysis of human diseasesR35GM149527 · NIGMS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Yufeng Shen · 2023 to 2026
$1.6M
NIGMS NIH HHS R35 GM149527
6 · The paper itself

Abstract

Structural dynamics are fundamental to protein functions and mutation effects. Current protein deep learning models are predominantly trained on sequence and/or static structure data, which often fail to capture the dynamic nature of proteins. To address this, we introduce SeqDance and ESMDance, two protein language models trained on dynamic biophysical properties derived from molecular dynamics simulations and normal mode analyses of over 64,000 proteins. SeqDance, trained from scratch, learns both local dynamic interactions and global conformational properties for ordered and disordered proteins. SeqDance predicted dynamic property changes reflect mutation effect on protein folding stability. ESMDance, built upon ESM2 outputs, substantially outperforms ESM2 in zero-shot prediction of mutation effects for designed and viral proteins which lack evolutionary information. Together, SeqDance and ESMDance offer a new framework for integrating protein dynamics into language models, enabling more generalizable predictions of protein behavior and mutation effects.

Indexed as

molecular dynamicsmutation effectsnormal mode analysisprotein language model

Identifiers

PMID39464109
PMCPMC11507661

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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Registered trials

None linked

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.