Authors
Hu, Q., Mer, G.
Abstract
Cryo-electron microscopy (cryo-EM) and cryo-electron tomography (cryo-ET) can yield density maps whose molecular identities are unknown. Predicted-structure databases enable proteome-scale searches, but distinguishing the correct candidates remains challenging, particularly for intermediate-resolution maps without clear side-chain features. We developed CryoAssign, an automated framework that combines large-scale structure matching with learning-to-rank prioritization. CryoAssign searches intact density maps without prior segmentation and integrates complementary measures of map-model agreement. On held-out benchmark maps, CryoAssign robustly prioritized the correct candidates. It also identified proteins or narrowed the set of candidates in previously unassigned cryo-EM maps and recovered multiple components from complex cryo-EM and cryo-ET maps. Controlled low-pass filtering showed generally robust recovery across a broad range of intermediate resolutions. CryoAssign provides a scalable approach for identifying proteins from cryo-EM and cryo-ET density maps.
Preprint server:
bioRxiv
The authors list and abstract were imported from bioRxiv on 14 Oct 2026.
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