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ACS Omega· 2026Q1

Deep Learning for Protein Secondary-Structure Segmentation in Intermediate-Resolution Cryo-EM Maps: A Resolution-Stratified Benchmark Dataset and Controlled Evaluation

Md Ehashan Rabbi Pial, Farhan Noor Dehan, Salim Sazzed

Short summary

Residual U-Net achieved the highest segmentation accuracy (Macro-FG F1 score) for protein secondary structures (helices, sheets, NPSS) in intermediate-resolution cryo-EM maps (4.5–8.0 Å), with performance consistently improving at higher resolutions within this range.

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Key points

  • A new resolution-stratified benchmark dataset (4.5–8.0 Å) with voxel-level annotations for helices, sheets, and NPSS regions was created from 972 protein-chain samples.
  • Residual U-Net achieved the highest Macro-FG F1 score for secondary-structure segmentation in all three resolution bins (4.5–5.5, 5.5–6.5, 6.5–8.0 Å).
  • Segmentation accuracy for all five evaluated architectures (U-Net, Residual U-Net, Attention U-Net, UNETR, Swin-UNETR) improved with higher resolution maps.
  • Helices were segmented more accurately than sheets and NPSS regions across all models and resolution bins.

AI-generated from the title and abstract; the full text is not read.

Abstract

Abstract Accurate segmentation of protein secondary structures in cryo-electron microscopy (cryo-EM) maps is crucial for protein tracing and atomic model building, yet remains challenging at intermediate resolutions. Although deep learning architectures have recently been applied to this task, there remains a lack of standardized evaluation protocols and systematic resolution-stratified analyses. Consequently, it remains unclear how segmentation performance varies across finer resolution ranges within the intermediate-resolution regime and how different volumetric segmentation architectures compare under controlled experimental conditions. To address these gaps, we present a nonredundant, resolution-stratified benchmark dataset and a controlled evaluation framework for protein secondary-structure segmentation in intermediate-resolution cryo-EM maps. The dataset comprises 972 nonredundant protein-chain samples from 495 cryo-EM protein structures resolved at 4.5–8.0 Å, with voxel-level annotations for helices, sheets, and non-periodic secondary-structure (NPSS) regions. The dataset is stratified into three resolution ranges─4.5–5.5, 5.5–6.5, and 6.5–8.0 Å─to enable systematic analysis of resolution-dependent segmentation performance. Using this benchmark, we evaluate five representative convolutional and transformer-based volumetric segmentation architectures─U-Net, Residual U-Net, Attention U-Net, UNETR, and Swin-UNETR─under standardized preprocessing, training, and evaluation protocols. Residual U-Net achieves the highest macro-averaged foreground (Macro-FG) F1 score in all three resolution bins, while helices are segmented more accurately than sheets and NPSS regions. All five architectures achieve their highest Macro-FG F1 scores in the highest-resolution bin, whereas performance varies between the two lower-resolution bins across architectures and secondary-structure classes. Overall, this benchmark enables fine-grained analysis of resolution-dependent segmentation performance, supports reproducible method development, and facilitates controlled comparison of future cryo-EM secondary-structure segmentation approaches.

The authors' abstract, as published at the source. ACS Omega, 2026 · DOI ↗

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Structural BiologyBiochemistry, Genetics and Molecular Biology