Skip to content

LumiCharge: Spherical Harmonic Convolutional Networks for Atomic Charge Prediction in Drug Discovery.

Jun 2025 · Journal of Physical Chemistry Letters · Vol 16, pp. 6334-6344 · 2 citations · 36 references
Medicine

TL;DR

This work proposes LumiCharge, a novel atomic charge prediction framework that incorporates high-order spherical harmonics convolutions and explicitly models multibody interactions, and demonstrates exceptional extrapolation capability and robustness across molecules of varying sizes, effectively overcoming the limitations imposed by molecular sizes.

Abstract

Atomic charge is crucial in drug design for analyzing reactive sites and interactions between ligands and targets. While quantum mechanical methods offer high accuracy, they are generally computationally costly. Conversely, empirical approaches, while computationally efficient, frequently suffer from lack of precision and generalizability. Recent a number of machine learning-based models have been developed for atomic charge predictions, but they struggle with accurately representing molecular structures and capturing the chemical environments affecting atomic charges, thus limiting their generalization and accuracy. To overcome these limitations, we propose LumiCharge, a novel atomic charge prediction framework that incorporates high-order spherical harmonics convolutions and explicitly models multibody interactions. In constructing this model, we employ a strategy that integrates both high- and low-order information, enhancing its geometric spatial perception capability, which is currently underexplored in the field. Benchmark evaluations demonstrate that LumiCharge outperforms state-of-the-art (SOTA) models by 30%-60% across diverse data sets. Additionally, in cross-scale experiments, LumiCharge demonstrates exceptional extrapolation capability and robustness across molecules of varying sizes, effectively overcoming the limitations imposed by molecular sizes. On an external halogen-containing test set, LumiCharge achieves an RMSE of 0.055e, meeting practical application requirements. Finally, a case study of virtual screening for the androgen receptor (AR) target further validates its outstanding accuracy compared to the OPLS3e force field and other deep learning (DL)-based baseline models, highlighting its exceptional generalization capacity and practical utility in real-world scenarios.

View source

Similar papers

Aug 2026

Δ -Machine Learning for the Prediction of Metal Complex Properties.

An adaptation of the Δ-ML strategy for quantum property prediction of transition metal complexes is presented, which consistently achieves higher accuracy in the prediction of high-fidelity targets, while demonstrating improved data efficiency and out-of-domain transferability.

Hannes Kneiding, David Balcells · 0 citations
#protein folding Conference Open access Sep 2026

Evaluating the Transferability and Distinguishability of Atomic Moments Across Atom in Molecule (AIM) Partitioning Schemes

By identifying AIM methods that result in conformationally stable and transferable atomic properties, this study aims to improve IDP modelling and guide the development of more accurate force fields for biologically relevant systems.

Emily Machel, Farnaz Heidar-Zadeh, Negar Molavi et al. · 0 citations
Jul 2026

A Scalable Structure-Aware Multimodal Architecture for Accurate Drug-Target Affinity Prediction.

Accurate prediction of drug-target binding affinity (DTA) is a key task in virtual screening. However, current computational methods face a key challenge: sequence-based approaches often fail to capture critical spatial information, while structure-based models rely on computationally expensive 3D coordinates, which restrict their scalability. To address this issue, we propose StructuraDTA, a novel multimodal framework that adopts an implicit structure modeling strategy. Instead of using static protein folding data, our method encodes drug molecular graphs via Graph Isomorphism Networks (GINs) to capture fine-grained topological features. Meanwhile, we optimize protein representations by integrating probabilistic structural priors into a pretrained language model, which effectively simulates thermodynamic conformational flexibility without relying on explicit 3D structural data. A bidirectional cross-attention mechanism is then used to dynamically align these heterogeneous feature modalities. Comprehensive evaluations on the Davis and KIBA benchmark datasets show that StructuraDTA stably outperforms state of-the-art comparison methods. Importantly, the model exhibits strong robustness in cold-start scenarios, and can accurately predict binding affinities for previously unseen drugs and targets. By retaining the predictive performance of structure based models while maintaining the high inference efficiency of sequence-based methods, we provide an accurate and scalable solution to accelerate genome-scale drug discovery research.

Junlin Xu, Ye Yuan, Menglong Hu et al. · 0 citations
Open access Aug 2026

Modeling dual-range atomic interactions with physicochemical principles for molecular force fields

GeoNet is a physicochemical-principle-guided framework for modeling dual-range atomic interactions that achieves the smallest model size and the shortest training time, demonstrating both superior predictive performance and computational efficiency.

Honghao Wang, Zunlong Liu, Xiangxiang Zeng et al. · 0 citations
Aug 2026

Molecular Property Prediction via Sparse Binary Matrix Representation and Convolutional Neural Networks

The SBMR-CNN model demonstrates highly competitive accuracy, outperforming the CM, Uni-Mol+, and MPNN-2D benchmarks, while closely approaching the performance of the more computationally intensive MPNN-3D and SOAP descriptors, as well as the RF-MF model.

Abdulaziz W. Alherz, C. Tezak, Mohammed S. Alhajeri · 0 citations
Preprint Jul 2026

Rem3Di: Learning smooth, chiral 3D molecular descriptors from atomistic foundation models

Rem3Di is introduced, a representation-learning framework that repurposes latent features from atomistic foundation models as transferable molecular descriptors for property prediction and virtual screening and provides a route from simulation-trained atomistic representations to transferable, chirality-aware molecular representations for chemical machine learning.

Steffen Wedig, Felix Burton, Rokas Elijošius et al. · 0 citations

Related blog posts

GPT-Lab Aug 28, 2026

We built an AI factory for HVAC control

What does it take to trust AI-driven HVAC optimization? Our AI Model Factory combines agents, machine learning, reinforcement learning and deterministic checks in a governed workflow designed for messy, real-world building data. The post We built an AI factory for HVAC control appeared first on GPT-Lab.

Microsoft Research Blog Jul 30, 2026

EvoLib: Turning experience into evolving knowledge

LLMs do not get smarter just by remembering more. EvoLib turns experience into evolving knowledge, taking reusable skills and insights that help models learn and adapt across tasks long after deployment. The post EvoLib: Turning experience into evolving knowledge appeared first on Microsoft Research.

We use cookies to run the site and, with your consent, for analytics and to show ads. See our Cookie Policy.