GEM-2: Next Generation Molecular Property Prediction Network by Modeling Full-range Many-body Interactions

Bibliographic Details
Title: GEM-2: Next Generation Molecular Property Prediction Network by Modeling Full-range Many-body Interactions
Authors: Liu, Lihang, He, Donglong, Fang, Xiaomin, Zhang, Shanzhuo, Wang, Fan, He, Jingzhou, Wu, Hua
Publication Year: 2022
Collection: Computer Science
Physics (Other)
Quantitative Biology
Subject Terms: Computer Science - Machine Learning, Physics - Chemical Physics, Quantitative Biology - Molecular Networks, Quantitative Biology - Quantitative Methods
More Details: Molecular property prediction is a fundamental task in the drug and material industries. Physically, the properties of a molecule are determined by its own electronic structure, which is a quantum many-body system and can be exactly described by the Schr"odinger equation. Full-range many-body interactions between electrons have been proven effective in obtaining an accurate solution of the Schr"odinger equation by classical computational chemistry methods, although modeling such interactions consumes an expensive computational cost. Meanwhile, deep learning methods have also demonstrated their competence in molecular property prediction tasks. Inspired by the classical computational chemistry methods, we design a novel method, namely GEM-2, which comprehensively considers full-range many-body interactions in molecules. Multiple tracks are utilized to model the full-range interactions between the many-bodies with different orders, and a novel axial attention mechanism is designed to approximate the full-range interaction modeling with much lower computational cost. Extensive experiments demonstrate the overwhelming superiority of GEM-2 over multiple baseline methods in quantum chemistry and drug discovery tasks. The ablation studies also verify the effectiveness of the full-range many-body interactions.
Document Type: Working Paper
Access URL: http://arxiv.org/abs/2208.05863
Accession Number: edsarx.2208.05863
Database: arXiv
More Details
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