Evidence map›Paper›PMID 40465628›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2025

Amortized template matching of molecular conformations from cryoelectron microscopy images using simulation-based inference.

Lars Dingeldein, David Silva-Sánchez, Luke Evans, Edoardo D'Imprima, Nikolaus Grigorieff, Roberto Covino, Pilar Cossio

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Improving Conformational Ensembles of Folded Proteins in Go̅Martini.Journal of chemical theory and computation · 2026
    Article
  6. Article
  7. Amortized template matching of molecular conformations from cryoelectron microscopy images using simulation-based inference.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  8. InstaMap: instant-NGP for cryo-EM density maps.Acta crystallographica. Section D, Structural biology · 2025
    Article
  9. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Lars DingeldeinInstitute of Physics, Faculty of Physics, Goethe University Frankfurt, Frankfurt am Main 60438, Germany.
David Silva-SánchezDepartment of Applied Mathematics, Yale University, New Haven, CT 06520.
Luke EvansCenter for Computational Mathematics, Flatiron Institute, New York, NY 10010.ORCID 0000-0003-1683-503X
Edoardo D'ImprimaIstituto di Ricovero e Cura a Carattere Scientifico Humanitas Research Hospital, Unit of Correlative Light Emission Microscopy Core, Rozzano, Milan 20089, Italy.ORCID 0000-0002-9830-7929
Nikolaus GrigorieffRNA Therapeutics Institute, University of Massachusetts Chan Medical School, Worcester, MA 01605.ORCID 0000-0002-1506-909X
Roberto CovinoFrankfurt Institute for Advanced Studies, Frankfurt am Main 60438, Germany.ORCID 0000-0003-0884-0402
Pilar CossioCenter for Computational Mathematics, Flatiron Institute, New York, NY 10010.ORCID 0000-0002-5404-9948

Funding

Goethe-Universität Frankfurt am Main (Goethe-Universität)Howard Hughes Medical Institute (HHMI)LOEWE Zentrum AdRIA (AdRIA)Simons Foundation (SF)
6 · The paper itself

Abstract

Characterizing the conformational ensemble of biomolecular systems is key to understand their functions. Cryoelectron microscopy (cryo-EM) captures two-dimensional snapshots of biomolecular ensembles, giving in principle access to thermodynamics. However, these images are very noisy and show projections of the molecule in unknown orientations, making it very difficult to identify the biomolecule's conformation in each individual image. Here, we introduce cryo-EM simulation-based inference (cryoSBI) to infer the conformations of biomolecules and the uncertainties associated with the inference from individual cryo-EM images. CryoSBI builds on simulation-based inference, a merger of physics-based simulations and probabilistic deep learning, allowing us to use Bayesian inference even when likelihoods are too expensive to calculate. We begin with an ensemble of conformations, templates from experiments, and molecular modeling, serving as structural hypotheses. We train a neural network approximating the Bayesian posterior using simulated images from these templates and then use it to accurately infer the conformation of the biomolecule from each experimental image. Training is only done once on simulations, and after that, it takes just a few milliseconds to make inference on an image, making cryoSBI suitable for arbitrarily large datasets and direct analysis on micrographs. CryoSBI eliminates the need to estimate particle pose and imaging parameters, significantly enhancing the computational speed compared to explicit likelihood methods. Importantly, we obtain interpretable machine learning models by integrating physics-based approaches with deep neural networks, ensuring that our results are transparent and reliable. We illustrate and benchmark cryoSBI on synthetic data and showcase its promise on experimental single-particle cryo-EM data.

Indexed as

Cryoelectron MicroscopyImage Processing, Computer-AssistedMolecular ConformationBayes TheoremComputer SimulationDeep LearningModels, MolecularNeural Networks, ComputerBayesian inferencebiophysicscryo-EMmodelingtemplate matching

Identifiers

PMID40465628
PMCPMC12168013

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.