Evidence map›Paper›PMID 39044842›Full record

ArticleFrontiers in molecular biosciences2024

Towards interpretable Cryo-EM: disentangling latent spaces of molecular conformations.

David A Klindt, Aapo Hyvärinen, Axel Levy, Nina Miolane, Frédéric Poitevin

Abstract read
In one paragraph

Article in Frontiers in molecular biosciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. 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
  3. Article
  4. InstaMap: instant-NGP for cryo-EM density maps.Acta crystallographica. Section D, Structural biology · 2025
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

David A KlindtLCLS, SLAC National Accelerator Laboratory, Stanford University, Palo Alto, CA, United States.
Aapo HyvärinenDepartment of Computer Science, University of Helsinki, Helsinki, Finland.
Axel LevyLCLS, SLAC National Accelerator Laboratory, Stanford University, Palo Alto, CA, United States.
Nina MiolaneDepartment of Electrical and Computer Engineering, University of California Santa Barbara (UCSB), Santa Barbara, CA, United States.
Frédéric PoitevinLCLS, SLAC National Accelerator Laboratory, Stanford University, Palo Alto, CA, United States.

Funding

Improving membrane proteins' 3D reconstructions with cryo-electron microscopyR01GM144965 · NIGMS · UNIVERSITY OF CALIFORNIA SANTA BARBARA · PI MIOLANE, NINA · 2021 to 2023
$600k
NIGMS NIH HHS R01 GM144965
6 · The paper itself

Abstract

Molecules are essential building blocks of life and their different conformations (i.e., shapes) crucially determine the functional role that they play in living organisms. Cryogenic Electron Microscopy (cryo-EM) allows for acquisition of large image datasets of individual molecules. Recent advances in computational cryo-EM have made it possible to learn latent variable models of conformation landscapes. However, interpreting these latent spaces remains a challenge as their individual dimensions are often arbitrary. The key message of our work is that this interpretation challenge can be viewed as an Independent Component Analysis (ICA) problem where we seek models that have the property of identifiability. That means, they have an essentially unique solution, representing a conformational latent space that separates the different degrees of freedom a molecule is equipped with in nature. Thus, we aim to advance the computational field of cryo-EM beyond visualizations as we connect it with the theoretical framework of (nonlinear) ICA and discuss the need for identifiable models, improved metrics, and benchmarks. Moving forward, we propose future directions for enhancing the disentanglement of latent spaces in cryo-EM, refining evaluation metrics and exploring techniques that leverage physics-based decoders of biomolecular systems. Moreover, we discuss how future technological developments in time-resolved single particle imaging may enable the application of nonlinear ICA models that can discover the true conformation changes of molecules in nature. The pursuit of interpretable conformational latent spaces will empower researchers to unravel complex biological processes and facilitate targeted interventions. This has significant implications for drug discovery and structural biology more broadly. More generally, latent variable models are deployed widely across many scientific disciplines. Thus, the argument we present in this work has much broader applications in AI for science if we want to move from impressive nonlinear neural network models to mathematically grounded methods that can help us learn something new about nature.

Indexed as

AI for sciencecryo-EMdisentanglementICAmachine learningphysics-based models

Identifiers

PMID39044842
PMCPMC11263974

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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.