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RevGraphVAMP: A protein molecular simulation analysis model combining graph convolutional neural networks and physical constraints.

Authors :
Huang, Ying
Zhang, Huiling
Lin, Zhenli
Wei, Yanjie
Xi, Wenhui
Source :
Methods. Sep2024, Vol. 229, p163-174. 12p.
Publication Year :
2024

Abstract

• Effective degradation and state transition prediction of protein molecular simulation trajectories. • Integrate graph convolutional neural networks and physical constraint optimization. • Provides interpretable results on the importance of protein molecules. Molecular dynamics simulation is a crucial research domain within the life sciences, focusing on comprehending the mechanisms of biomolecular interactions at atomic scales. Protein simulation, as a critical subfield, often utilizes MD for implementation, with trajectory data play a pivotal role in drug discovery. The advancement of high-performance computing and deep learning technology becomes popular and critical to predict protein properties from vast trajectory data, posing challenges regarding data features extraction from the complicated simulation data and dimensionality reduction. Simultaneously, it is essential to provide a meaningful explanation of the biological mechanism behind dimensionality. To tackle this challenge, we propose a new unsupervised model named RevGraphVAMP to intelligently analyze the simulation trajectory. This model is based on the variational approach for Markov processes (VAMP) and integrates graph convolutional neural networks and physical constraint optimization to enhance the learning performance. Additionally, we introduce attention mechanism to assess the importance of key interaction region, facilitating the interpretation of molecular mechanism. In comparison to other VAMPNets models, our model showcases competitive performance, improved accuracy in state transition prediction, as demonstrated through its application to two public datasets and the Shank3-Rap1 complex, which is associated with autism spectrum disorder. Moreover, it enhanced dimensionality reduction discrimination across different substates and provides interpretable results for protein structural characterization. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
10462023
Volume :
229
Database :
Academic Search Index
Journal :
Methods
Publication Type :
Academic Journal
Accession number :
178735404
Full Text :
https://doi.org/10.1016/j.ymeth.2024.06.011