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arXiv:cs.AI· Advaith Maddipatla, M\"art-Erik M\"aeots, Marco Pegoraro, Nikolaus Dr\"ager, Roberto Covino, Sanketh Vedula, Martin Pacesa, Alex M. Bronstein·· 4 小时前AI 评分37

Fold'EM:从 Cryo-EM 粒子图像直接推断原子结构

Fold'EM: Direct atomic structure inference from Cryo-EM particles

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Fold'EM 是一个推理时框架,将蛋白质生成模型的先验直接与 cryo-EM 粒子图像结合,绕过密度重建和下游原子模型构建,从少量单粒子图像中确定原子结构。在合成与实验数据集上,该方法在已知粒子取向和取向与结构联合推断的 ab-initio 场景下均能恢复准确原子结构,并在异质数据集中直接解析不同构象状态。

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Abstract:Single-particle cryo-electron microscopy (cryo-EM) has become a widely adopted technique for biomolecular structure determination. The conventional cryo-EM computational pipeline first combines many particle images to reconstruct an electrostatic potential (ESP) map and then fits an atomic model to the recovered map. Density reconstruction has high sample complexity, requiring large numbers of particle images and making structure determination high-cost and low-throughput, particularly for heterogeneous samples. Downstream atomic model building, in turn, becomes increasingly difficult as the resolution of the reconstructed map deteriorates. Protein structure prediction models provide strong sequence-derived priors on atomic structure, and experiment-guided approaches can use these priors to recover structures consistent with experimental measurements. Yet, in cryo-EM, such priors are typically integrated only after density reconstruction during atomic model fitting. We introduce Fold'EM, an inference-time framework that combines priors from protein generative models directly with cryo-EM particle images to determine atomic models from a small number of single particle images, bypassing both intermediate density reconstruction and downstream model building against the reconstructed map. Across synthetic and experimental cryo-EM datasets, Fold'EM recovers accurate atomic structures both with known particle orientations and in an ab-initio setting where orientations are inferred jointly with structure. In heterogeneous datasets, Fold'EM further resolves distinct conformational states from mixed particle populations without separately reconstructing a density map and building an atomic model for each state. We believe these results open new avenues for structure determination in the low-sample regime and for characterizing low-population conformational states directly from cryo-EM particles.
Subjects: Biomolecules (q-bio.BM); Artificial Intelligence (cs.AI)
Cite as: arXiv:2610.01358 [q-bio.BM]
  (or arXiv:2610.01358v2 [q-bio.BM] for this version)
  https://doi.org/10.48550/arXiv.2610.01358

arXiv-issued DOI via DataCite

Submission history

From: Sai Advaith Maddipatla [view email]
[v1] Thu, 1 Oct 2026 09:28:37 UTC (18,477 KB)
[v2] Fri, 2 Oct 2026 09:45:31 UTC (13,097 KB)

来源:arXiv:cs.AI · arxiv.org