A practical framework for rapid calculation of protein polarization energies with anisotropic atomic polarizabilities

An accurate description of electronic polarization is fundamental to modeling protein interactions and dynamics. Despite its importance, polarization is frequently omitted in classical force fields, while existing polarizable models are hindered by parameterization complexity, high computational cost, or limited resolution. We present a novel, efficient method for calculating protein polarization energies. Our method computes local electric fields at atomic sites, decomposes them into bond-parallel and perpendicular components, and uses environment-specific, anisotropic atomic polarizabilities fitted to accurate quantum-chemical calculations. The model accurately reproduces quantum-mechanical polarization energies for amino-acid monomers, dimers, trimers, and small proteins. Its computational efficiency enables application to large, explicitly solvated proteins, achieving excellent agreement with benchmark data at a minimal computational cost. We demonstrate its scalability by applying it to large, solvated proteins, providing a practical path for incorporating polarization into biomolecular simulations.

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Publication Details

Journal
The Journal of Chemical Physics
Published
2026-02-05
DOI
https://doi.org/10.1063/5.0315855
Primary Topic
Protein Structure and Dynamics
Type
article
Field-Weighted Citation Impact
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article

A practical framework for rapid calculation of protein polarization energies with anisotropic atomic polarizabilities

Wan-Sheng Ren, Jin Xiao, John Z. H. Zhang, Tong Zhu et al.
The Journal of Chemical Physics
Protein Structure and Dynamics
article

A practical framework for rapid calculation of protein polarization energies with anisotropic atomic polarizabilities

Wan-Sheng Ren, Jin Xiao, John Z. H. Zhang, Tong Zhu, Yingfeng Zhang
article en

Abstract

An accurate description of electronic polarization is fundamental to modeling protein interactions and dynamics. Despite its importance, polarization is frequently omitted in classical force fields, while existing polarizable models are hindered by parameterization complexity, high computational cost, or limited resolution. We present a novel, efficient method for calculating protein polarization energies. Our method computes local electric fields at atomic sites, decomposes them into bond-parallel and perpendicular components, and uses environment-specific, anisotropic atomic polarizabilities fitted to accurate quantum-chemical calculations. The model accurately reproduces quantum-mechanical polarization energies for amino-acid monomers, dimers, trimers, and small proteins. Its computational efficiency enables application to large, explicitly solvated proteins, achieving excellent agreement with benchmark data at a minimal computational cost. We demonstrate its scalability by applying it to large, solvated proteins, providing a practical path for incorporating polarization into biomolecular simulations.

The Journal of Chemical PhysicsVol. 164(5)
Shanxi University (CN), New York University Shanghai (CN), Shanghai Innovative Research Center of Traditional Chinese Medicine (CN), Institute for History of Natural Sciences (CN), Shenzhen Technology University (CN), New York University (US), East China Normal University (CN)
Affordable and clean energy
Openalex Percentile: Top 66%
Protein Structure and Dynamics
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