用深度学习+AlphaFold提升低分辨率冷冻电镜图的蛋白结构预测精度
Beyond Current Boundaries: Integrating Deep Learning and AlphaFold for Enhanced Protein Structure Prediction from Low-Resolution Cryo-EM Maps
- 融合深度学习与AlphaFold,先优化低分辨率电镜图再建模
- 95.5%低分辨率图中预测残基数显著增加,模型更完整
- 适合做冷冻电镜结构解析的研究者,尤其擅长低分辨数据
从冷冻电镜(cryo-EM)图构建原子模型是结构生物学中的关键但复杂任务。尽管深度学习方法如卷积神经网络(CNN)和图神经网络(GNN)推动了DeepTracer、ModelAngelo等先进图到模型工具的发展,但在分辨率超过4 Å的低分辨率图上效果明显下降。为解决此问题,我们提出DeepTracer-LowResEnhance框架,结合深度学习增强的图精炼技术与AlphaFold的强大能力,显著提升低分辨率图的建模性能。该方法在37个蛋白的冷冻电镜图上进行了测试,分辨率范围为2.5至8.4 Å,其中22个低于4 Å。结果表明,95.5%的低分辨率图中预测残基数显著增加,显示原子模型构建能力大幅提升。与Phenix自动锐化功能对比显示,DeepTracer-LowResEnhance能生成更细致、更精确的原子模型,突破当前计算结构生物学方法的边界。
原文摘要 · Abstract (English)
Constructing atomic models from cryo-electron microscopy (cryo-EM) maps is a crucial yet intricate task in structural biology. While advancements in deep learning, such as convolutional neural networks (CNNs) and graph neural networks (GNNs), have spurred the development of sophisticated map-to-model tools like DeepTracer and ModelAngelo, their efficacy notably diminishes with low-resolution maps beyond 4 Å. To address this shortfall, our research introduces DeepTracer-LowResEnhance, an innovative framework that synergizes a deep learning-enhanced map refinement technique with the power of AlphaFold. This methodology is designed to markedly improve the construction of models from low-resolution cryo-EM maps. DeepTracer-LowResEnhance was rigorously tested on a set of 37 protein cryo-EM maps, with resolutions ranging between 2.5 to 8.4 Å, including 22 maps with resolutions lower than 4 Å. The outcomes were compelling, demonstrating that 95.5\% of the low-resolution maps exhibited a significant uptick in the count of total predicted residues. This denotes a pronounced improvement in atomic model building for low-resolution maps. Additionally, a comparative analysis alongside Phenix's auto-sharpening functionality delineates DeepTracer-LowResEnhance's superior capability in rendering more detailed and precise atomic models, thereby pushing the boundaries of current computational structural biology methodologies.
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