Angular Deviation Diffuser: A Transformer-Based Diffusion Model for Efficient Protean Conformational Ensemble Generation

Protein functionality is inherently tied to its structure, with both static and dynamic conformations playing critical roles in defining biological activity. While molecular dynamics (MD) simulations have long been the standard for exploring protein dynamics, they come with high computational costs and limited sampling efficiency. Recent advances in deep learning, such as AlphaFold, have significantly improved static protein structure prediction, yet accurately generating the dynamic ensemble of protein conformations remains a complex challenge. In this thesis, we present a transformer-based diffusion model that generates diverse conformational ensembles of protein backbones by utilizing angular deviations as data flow. Our model combines a cutting-edge diffusion model with the principles of SE(3) symmetry to enhance both the accuracy and efficiency of conformational sampling. Applied to the Vivid (VVD) Photoreceptor protein system, the generated ensembles closely align with those from MD simulations while covering a broader range of conformational states. This approach offers an improved methodology for capturing protein dynamics, contributing to a more comprehensive understanding of protein structure and function.

Publication Details

Journal
SMU Scholar (Southern Methodist University)
Published
2024-12-21
Primary Topic
Magnetic confinement fusion research
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article
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article

Angular Deviation Diffuser: A Transformer-Based Diffusion Model for Efficient Protean Conformational Ensemble Generation

SMU Scholar (Southern Methodist University)
Magnetic confinement fusion research
article

Angular Deviation Diffuser: A Transformer-Based Diffusion Model for Efficient Protean Conformational Ensemble Generation

article en

Abstract

Protein functionality is inherently tied to its structure, with both static and dynamic conformations playing critical roles in defining biological activity. While molecular dynamics (MD) simulations have long been the standard for exploring protein dynamics, they come with high computational costs and limited sampling efficiency. Recent advances in deep learning, such as AlphaFold, have significantly improved static protein structure prediction, yet accurately generating the dynamic ensemble of protein conformations remains a complex challenge. In this thesis, we present a transformer-based diffusion model that generates diverse conformational ensembles of protein backbones by utilizing angular deviations as data flow. Our model combines a cutting-edge diffusion model with the principles of SE(3) symmetry to enhance both the accuracy and efficiency of conformational sampling. Applied to the Vivid (VVD) Photoreceptor protein system, the generated ensembles closely align with those from MD simulations while covering a broader range of conformational states. This approach offers an improved methodology for capturing protein dynamics, contributing to a more comprehensive understanding of protein structure and function.

SMU Scholar (Southern Methodist University)
Openalex Percentile: Top 29%
Magnetic confinement fusion research
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