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Record W4407545139 · doi:10.1021/acs.jctc.4c01406

Nonbonded Force Field Parameters Derived from Atoms-in-Molecules Methods Reproduce Interactions in Proteins from First-Principles

2025· article· en· W4407545139 on OpenAlexafffund
Carlos Castillo-Orellana, Farnaz Heidar‐Zadeh, Esteban Vöhringer‐Martinez

Bibliographic record

VenueJournal of Chemical Theory and Computation · 2025
Typearticle
Languageen
FieldPhysics and Astronomy
TopicForce Microscopy Techniques and Applications
Canadian institutionsQueen's University
FundersAlliance de recherche numérique du CanadaFondo Nacional de Desarrollo Científico y TecnológicoAgencia Nacional de Investigación y DesarrolloMax-Planck-GesellschaftNatural Sciences and Engineering Research Council of CanadaQueen's University
KeywordsForce field (fiction)Field (mathematics)MoleculeChemical physicsNanotechnologyPhysicsComputational chemistryComputer scienceStatistical physicsChemistryMaterials scienceQuantum mechanicsMathematics

Abstract

fetched live from OpenAlex

Noncovalent interactions govern many chemical and biological phenomena and are crucial in protein–protein interactions, enzyme catalysis, and DNA folding. The size of these macromolecules and their various conformations demand computationally inexpensive force fields that can accurately mimic the quantum chemical nature of the atomic noncovalent interactions. Accurate force fields, coupled with increasingly longer molecular dynamics simulations, may empower us to predict conformational changes associated with the biochemical function of proteins. Here, we aim to derive nonbonded protein force field parameters from the partitioned electron density of amino acids, the fundamental units of proteins, via the atoms-in-molecules (AIM) approach. The AIM parameters are validated using a database of charged, aromatic, and hydrophilic side-chain interactions in 610 conformations, primarily involving π–π interactions, as recently reported by one of us (Carter-Fenk et al., 2023). Electrostatic and van der Waals interaction energies calculated with nonbonded force field parameters from different AIM methodologies were compared to first-principles interaction energies from absolute localized molecular orbital-energy decomposition analysis (ALMO-EDA) at the ωB97XV/def2-TZVPD level. Our findings show that electrostatic interactions between side chains are accurately reproduced by atomic charges from the minimal basis iterative stockholder (MBIS) scheme with mean absolute errors of 4–7 kJ/mol. Meanwhile, C 6 coefficients from the MBIS AIM method effectively predict dispersion interactions with a mean error of −2 kJ/mol and a maximal error of −5 kJ/mol. As an outlook to use AIM methods in the development of protein force fields, we present the constrained AIM method that allows one to fix backbone parameters during the optimization of side-chain interactions. Backbone dihedral parameters have been optimized to reproduce secondary structure elements in proteins, and not altering them maintains compatibility with conventional protein force fields while improving the description of side-chain interactions. Our validated AIM methods allow for the depiction of noncovalent, long-range interactions in proteins using cost-effective force fields that achieve chemical precision.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.000
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Bench or experimental · Consensus signal: Bench or experimental
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.333
Threshold uncertainty score0.305

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0000.000
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0000.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.016
GPT teacher head0.346
Teacher spread0.330 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one teacher head, not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designBench or experimental
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations6
Published2025
Admission routes2
Has abstractyes

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