ProFusion: 3D Reconstruction of Protein Complex Structures from Multi-view AFM Images

Fuente: arXiv
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Autores principales: Rade, Jaydeep, Hasib, Md Hasibul Hasan, Ozturk, Meric, Faal, Baboucarr, Yang, Sheng, Sashital, Dipali G., Venditti, Vincenzo, Chen, Baoyu, Sarkar, Soumik, Krishnamurthy, Adarsh, Sarkar, Anwesha
Formato: Preprint
Publicado: 2025
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author Rade, Jaydeep
Hasib, Md Hasibul Hasan
Ozturk, Meric
Faal, Baboucarr
Yang, Sheng
Sashital, Dipali G.
Venditti, Vincenzo
Chen, Baoyu
Sarkar, Soumik
Krishnamurthy, Adarsh
Sarkar, Anwesha
author_facet Rade, Jaydeep
Hasib, Md Hasibul Hasan
Ozturk, Meric
Faal, Baboucarr
Yang, Sheng
Sashital, Dipali G.
Venditti, Vincenzo
Chen, Baoyu
Sarkar, Soumik
Krishnamurthy, Adarsh
Sarkar, Anwesha
contents AI-based in silico methods have improved protein structure prediction but often struggle with large protein complexes (PCs) involving multiple interacting proteins due to missing 3D spatial cues. Experimental techniques like Cryo-EM are accurate but costly and time-consuming. We present ProFusion, a hybrid framework that integrates a deep learning model with Atomic Force Microscopy (AFM), which provides high-resolution height maps from random orientations, naturally yielding multi-view data for 3D reconstruction. However, generating a large-scale AFM imaging data set sufficient to train deep learning models is impractical. Therefore, we developed a virtual AFM framework that simulates the imaging process and generated a dataset of ~542,000 proteins with multi-view synthetic AFM images. We train a conditional diffusion model to synthesize novel views from unposed inputs and an instance-specific Neural Radiance Field (NeRF) model to reconstruct 3D structures. Our reconstructed 3D protein structures achieve an average Chamfer Distance within the AFM imaging resolution, reflecting high structural fidelity. Our method is extensively validated on experimental AFM images of various PCs, demonstrating strong potential for accurate, cost-effective protein complex structure prediction and rapid iterative validation using AFM experiments.
format Preprint
id arxiv_https___arxiv_org_abs_2509_15242
institution arXiv
publishDate 2025
record_format arxiv
spellingShingle ProFusion: 3D Reconstruction of Protein Complex Structures from Multi-view AFM Images
Rade, Jaydeep
Hasib, Md Hasibul Hasan
Ozturk, Meric
Faal, Baboucarr
Yang, Sheng
Sashital, Dipali G.
Venditti, Vincenzo
Chen, Baoyu
Sarkar, Soumik
Krishnamurthy, Adarsh
Sarkar, Anwesha
Computer Vision and Pattern Recognition
AI-based in silico methods have improved protein structure prediction but often struggle with large protein complexes (PCs) involving multiple interacting proteins due to missing 3D spatial cues. Experimental techniques like Cryo-EM are accurate but costly and time-consuming. We present ProFusion, a hybrid framework that integrates a deep learning model with Atomic Force Microscopy (AFM), which provides high-resolution height maps from random orientations, naturally yielding multi-view data for 3D reconstruction. However, generating a large-scale AFM imaging data set sufficient to train deep learning models is impractical. Therefore, we developed a virtual AFM framework that simulates the imaging process and generated a dataset of ~542,000 proteins with multi-view synthetic AFM images. We train a conditional diffusion model to synthesize novel views from unposed inputs and an instance-specific Neural Radiance Field (NeRF) model to reconstruct 3D structures. Our reconstructed 3D protein structures achieve an average Chamfer Distance within the AFM imaging resolution, reflecting high structural fidelity. Our method is extensively validated on experimental AFM images of various PCs, demonstrating strong potential for accurate, cost-effective protein complex structure prediction and rapid iterative validation using AFM experiments.
title ProFusion: 3D Reconstruction of Protein Complex Structures from Multi-view AFM Images
topic Computer Vision and Pattern Recognition
url https://arxiv.org/abs/2509.15242