IDEAS home Printed from https://ideas.repec.org/a/nat/natcom/v16y2025i1d10.1038_s41467-025-62226-7.html
   My bibliography  Save this article

Scalable 3D reconstruction for X-ray single particle imaging with online machine learning

Author

Listed:
  • Jay Shenoy

    (Stanford University
    SLAC National Accelerator Laboratory)

  • Axel Levy

    (SLAC National Accelerator Laboratory
    Stanford University)

  • Kartik Ayyer

    (Max Planck Institute for the Structure and Dynamics of Matter
    Center for Free-Electron Laser Science
    The Hamburg Centre for Ultrafast Imaging)

  • Frédéric Poitevin

    (SLAC National Accelerator Laboratory)

  • Gordon Wetzstein

    (Stanford University)

Abstract

X-ray free-electron lasers offer unique capabilities for measuring the structure and dynamics of biomolecules, helping us understand the basic building blocks of life. Notably, high-repetition-rate free-electron lasers enable single particle imaging, where individual, weakly scattering biomolecules are imaged under near-physiological conditions with the opportunity to access fleeting states that cannot be captured in cryogenic or crystallized conditions. Existing X-ray single particle reconstruction algorithms, which estimate the particle orientation for each image independently, are slow and memory-intensive when handling the massive datasets generated by emerging free-electron lasers. Here, we introduce X-RAI (X-Ray single particle imaging with Amortized Inference), an online reconstruction framework that estimates the structure of 3D macromolecules from large X-ray single particle datasets. X-RAI consists of a convolutional encoder, which amortizes pose estimation over large datasets, as well as a physics-based decoder, which employs an implicit neural representation to enable high-quality 3D reconstruction in an end-to-end, self-supervised manner. We demonstrate that X-RAI achieves state-of-the-art performance for small-scale datasets in simulation and challenging experimental settings and demonstrate its unprecedented ability to process large datasets containing millions of diffraction images in an online fashion. These abilities signify a paradigm shift in X-ray single particle imaging towards real-time reconstruction.

Suggested Citation

  • Jay Shenoy & Axel Levy & Kartik Ayyer & Frédéric Poitevin & Gordon Wetzstein, 2025. "Scalable 3D reconstruction for X-ray single particle imaging with online machine learning," Nature Communications, Nature, vol. 16(1), pages 1-10, December.
  • Handle: RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-62226-7
    DOI: 10.1038/s41467-025-62226-7
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/s41467-025-62226-7
    File Function: Abstract
    Download Restriction: no

    File URL: https://libkey.io/10.1038/s41467-025-62226-7?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    References listed on IDEAS

    as
    1. Takanori Nakane & Abhay Kotecha & Andrija Sente & Greg McMullan & Simonas Masiulis & Patricia M. G. E. Brown & Ioana T. Grigoras & Lina Malinauskaite & Tomas Malinauskas & Jonas Miehling & Tomasz Ucha, 2020. "Single-particle cryo-EM at atomic resolution," Nature, Nature, vol. 587(7832), pages 152-156, November.
    2. D. Starodub & A. Aquila & S. Bajt & M. Barthelmess & A. Barty & C. Bostedt & J.D. Bozek & N. Coppola & R.B. Doak & S.W. Epp & B. Erk & L. Foucar & L. Gumprecht & C.Y. Hampton & A. Hartmann & R. Hartma, 2012. "Single-particle structure determination by correlations of snapshot X-ray diffraction patterns," Nature Communications, Nature, vol. 3(1), pages 1-7, January.
    3. Rui Xu & Huaidong Jiang & Changyong Song & Jose A. Rodriguez & Zhifeng Huang & Chien-Chun Chen & Daewoong Nam & Jaehyun Park & Marcus Gallagher-Jones & Sangsoo Kim & Sunam Kim & Akihiro Suzuki & Yuki , 2014. "Single-shot three-dimensional structure determination of nanocrystals with femtosecond X-ray free-electron laser pulses," Nature Communications, Nature, vol. 5(1), pages 1-9, September.
    4. Katherine Henzler-Wildman & Dorothee Kern, 2007. "Dynamic personalities of proteins," Nature, Nature, vol. 450(7172), pages 964-972, December.
    Full references (including those not matched with items on IDEAS)

    Most related items

    These are the items that most often cite the same works as this one and are cited by the same works as this one.
    1. Ninghai Gan & Weizhong Zeng & Yan Han & Qingfeng Chen & Youxing Jiang, 2024. "Structural mechanism of proton conduction in otopetrin proton channel," Nature Communications, Nature, vol. 15(1), pages 1-13, December.
    2. César Augusto F de Oliveira & Barry J Grant & Michelle Zhou & J Andrew McCammon, 2011. "Large-Scale Conformational Changes of Trypanosoma cruzi Proline Racemase Predicted by Accelerated Molecular Dynamics Simulation," PLOS Computational Biology, Public Library of Science, vol. 7(10), pages 1-7, October.
    3. Sean L Seyler & Avishek Kumar & M F Thorpe & Oliver Beckstein, 2015. "Path Similarity Analysis: A Method for Quantifying Macromolecular Pathways," PLOS Computational Biology, Public Library of Science, vol. 11(10), pages 1-37, October.
    4. Jonathan Schubert & Andrea Schulze & Chrisostomos Prodromou & Hannes Neuweiler, 2021. "Two-colour single-molecule photoinduced electron transfer fluorescence imaging microscopy of chaperone dynamics," Nature Communications, Nature, vol. 12(1), pages 1-12, December.
    5. Jiahua He & Tao Li & Sheng-You Huang, 2023. "Improvement of cryo-EM maps by simultaneous local and non-local deep learning," Nature Communications, Nature, vol. 14(1), pages 1-16, December.
    6. Alistair Bailey & Andy van Hateren & Tim Elliott & Jörn M Werner, 2014. "Two Polymorphisms Facilitate Differences in Plasticity between Two Chicken Major Histocompatibility Complex Class I Proteins," PLOS ONE, Public Library of Science, vol. 9(2), pages 1-11, February.
    7. Feiyu Zhao & Tao Zhang & Xiaodi Sun & Xiyun Zhang & Letong Chen & Hejun Wang & Jinze Li & Peng Fan & Liangxue Lai & Tingting Sui & Zhanjun Li, 2023. "A strategy for Cas13 miniaturization based on the structure and AlphaFold," Nature Communications, Nature, vol. 14(1), pages 1-13, December.
    8. Jing Cheng & Tong Liu & Xin You & Fa Zhang & Sen-Fang Sui & Xiaohua Wan & Xinzheng Zhang, 2023. "Determining protein structures in cellular lamella at pseudo-atomic resolution by GisSPA," Nature Communications, Nature, vol. 14(1), pages 1-9, December.
    9. Eike C. Schulz & Andreas Prester & David Stetten & Gargi Gore & Caitlin E. Hatton & Kim Bartels & Jan-Philipp Leimkohl & Hendrik Schikora & Helen M. Ginn & Friedjof Tellkamp & Pedram Mehrabi, 2025. "Probing the modulation of enzyme kinetics by multi-temperature, time-resolved serial crystallography," Nature Communications, Nature, vol. 16(1), pages 1-12, December.
    10. Lars V. Bock & Helmut Grubmüller, 2022. "Effects of cryo-EM cooling on structural ensembles," Nature Communications, Nature, vol. 13(1), pages 1-13, December.
    11. Yi-Ling Chen & Michael Habeck, 2017. "Data-driven coarse graining of large biomolecular structures," PLOS ONE, Public Library of Science, vol. 12(8), pages 1-17, August.
    12. repec:plo:pone00:0060553 is not listed on IDEAS
    13. Seonggon Lee & Hosung Ki & Donghwan Im & Jungmin Kim & Yunbeom Lee & Jain Gu & Alekos Segalina & Jun Heo & Yongjun Cha & Kyung Won Lee & Doyeong Kim & Jeongho Kim & Rory Ma & Jae Hyuk Lee & Hyotcherl , 2025. "Ultrafast structural dynamics of carbon–carbon single-bond rotation in transient radical species at non-equilibrium," Nature Communications, Nature, vol. 16(1), pages 1-12, December.
    14. repec:plo:pone00:0037399 is not listed on IDEAS
    15. Tobias Linder & Bert L de Groot & Anna Stary-Weinzinger, 2013. "Probing the Energy Landscape of Activation Gating of the Bacterial Potassium Channel KcsA," PLOS Computational Biology, Public Library of Science, vol. 9(5), pages 1-9, May.
    16. Sriram Aiyer & Philip R. Baldwin & Shi Min Tan & Zelin Shan & Juntaek Oh & Atousa Mehrani & Marianne E. Bowman & Gordon Louie & Dario Oliveira Passos & Selena Đorđević-Marquardt & Mario Mietzsch & Jos, 2024. "Overcoming resolution attenuation during tilted cryo-EM data collection," Nature Communications, Nature, vol. 15(1), pages 1-19, December.
    17. Teshani Kumarage & Sudipta Gupta & Nicholas B. Morris & Fathima T. Doole & Haden L. Scott & Laura-Roxana Stingaciu & Sai Venkatesh Pingali & John Katsaras & George Khelashvili & Milka Doktorova & Mich, 2025. "Cholesterol modulates membrane elasticity via unified biophysical laws," Nature Communications, Nature, vol. 16(1), pages 1-12, December.
    18. Laura Shub & Wenjin Liu & Georgios Skiniotis & Michael J. Keiser & Michael J. Robertson, 2025. "MIC: A deep learning tool for assigning ions and waters in cryo-EM and crystal structures," Nature Communications, Nature, vol. 16(1), pages 1-14, December.
    19. Yue Zhang & Biplob Nandy & Kasim Sader & Christopher J. Russo & Jan Löwe, 2025. "Foam film vitrification for cryo-EM," Nature Communications, Nature, vol. 16(1), pages 1-12, December.
    20. Markus Götz & Anders Barth & Søren S.-R. Bohr & Richard Börner & Jixin Chen & Thorben Cordes & Dorothy A. Erie & Christian Gebhardt & Mélodie C. A. S. Hadzic & George L. Hamilton & Nikos S. Hatzakis &, 2022. "A blind benchmark of analysis tools to infer kinetic rate constants from single-molecule FRET trajectories," Nature Communications, Nature, vol. 13(1), pages 1-12, December.
    21. Sheng Chen & Sen Zhang & Xiaoyu Fang & Liang Lin & Huiying Zhao & Yuedong Yang, 2024. "Protein complex structure modeling by cross-modal alignment between cryo-EM maps and protein sequences," Nature Communications, Nature, vol. 15(1), pages 1-14, December.
    22. Berk Küçükoğlu & Inayathulla Mohammed & Ricardo C. Guerrero-Ferreira & Stephanie M. Ribet & Georgios Varnavides & Max Leo Leidl & Kelvin Lau & Sergey Nazarov & Alexander Myasnikov & Massimo Kube & Jul, 2024. "Low-dose cryo-electron ptychography of proteins at sub-nanometer resolution," Nature Communications, Nature, vol. 15(1), pages 1-10, December.

    More about this item

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-62226-7. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    If CitEc recognized a bibliographic reference but did not link an item in RePEc to it, you can help with this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.