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Adaptive Ensemble Refinement of Protein Structures in High Resolution Electron Microscopy Density Maps with Radical Augmented Molecular Dynamics Flexible Fitting
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    Computational Biochemistry

    Adaptive Ensemble Refinement of Protein Structures in High Resolution Electron Microscopy Density Maps with Radical Augmented Molecular Dynamics Flexible Fitting
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    • Daipayan Sarkar*
      Daipayan Sarkar
      MSU-DOE Plant Research Laboratory, East Lansing, Michigan 48824, United States
      School of Molecular Sciences, Arizona State University, Tempe, Arizona 85281, United States
      *Email: [email protected]
    • Hyungro Lee
      Hyungro Lee
      Pacific Northwest National Laboratory, Richland, Washington 99354, United States
      Electrical & Computer Engineering, Rutgers University, New Brunswick, New Jersey 08854, United States
      More by Hyungro Lee
    • John W. Vant
      John W. Vant
      School of Molecular Sciences, Arizona State University, Tempe, Arizona 85281, United States
      More by John W. Vant
    • Matteo Turilli
      Matteo Turilli
      Electrical & Computer Engineering, Rutgers University, New Brunswick, New Jersey 08854, United States
      Computational Science Initiative, Brookhaven National Laboratory, Upton, New York 11973, United States
    • Josh V. Vermaas
      Josh V. Vermaas
      MSU-DOE Plant Research Laboratory, East Lansing, Michigan 48824, United States
    • Shantenu Jha*
      Shantenu Jha
      Electrical & Computer Engineering, Rutgers University, New Brunswick, New Jersey 08854, United States
      Computational Science Initiative, Brookhaven National Laboratory, Upton, New York 11973, United States
      *Email: [email protected]
      More by Shantenu Jha
    • Abhishek Singharoy*
      Abhishek Singharoy
      School of Molecular Sciences, Arizona State University, Tempe, Arizona 85281, United States
      *Email: [email protected]
    Other Access OptionsSupporting Information (1)

    Journal of Chemical Information and Modeling

    Cite this: J. Chem. Inf. Model. 2023, 63, 18, 5834–5846
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    https://doi.org/10.1021/acs.jcim.3c00350
    Published September 4, 2023
    Copyright © 2023 American Chemical Society

    Abstract

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    Recent advances in cryo-electron microscopy (cryo-EM) have enabled modeling macromolecular complexes that are essential components of the cellular machinery. The density maps derived from cryo-EM experiments are often integrated with manual, knowledge-driven or artificial intelligence-driven and physics-guided computational methods to build, fit, and refine molecular structures. Going beyond a single stationary-structure determination scheme, it is becoming more common to interpret the experimental data with an ensemble of models that contributes to an average observation. Hence, there is a need to decide on the quality of an ensemble of protein structures on-the-fly while refining them against the density maps. We introduce such an adaptive decision-making scheme during the molecular dynamics flexible fitting (MDFF) of biomolecules. Using RADICAL-Cybertools, the new RADICAL augmented MDFF implementation (R-MDFF) is examined in high-performance computing environments for refinement of two prototypical protein systems, adenylate kinase and carbon monoxide dehydrogenase. For these test cases, use of multiple replicas in flexible fitting with adaptive decision making in R-MDFF improves the overall correlation to the density by 40% relative to the refinements of the brute-force MDFF. The improvements are particularly significant at high, 2–3 Å map resolutions. More importantly, the ensemble model captures key features of biologically relevant molecular dynamics that are inaccessible to a single-model interpretation. Finally, the pipeline is applicable to systems of growing sizes, which is demonstrated using ensemble refinement of capsid proteins from the chimpanzee adenovirus. The overhead for decision making remains low and robust to computing environments. The software is publicly available on GitHub and includes a short user guide to install R-MDFF on different computing environments, from local Linux-based workstations to high-performance computing environments.

    Copyright © 2023 American Chemical Society

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    Supporting Information

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    The Supporting Information is available free of charge at https://pubs.acs.org/doi/10.1021/acs.jcim.3c00350.

    • Trace plot for the cross-correlation coefficient, calculated after every iteration in the R-MDFF protocol to fit ADK in high, intermediate, and low resolution electron denisty maps; MolProbity scores for models from R-MDFF trajectories and the performance of the R-MDFF algorithm when applied to larger biomolecular systems such as CODH; finally, the SI includes local cross correlation and SMOC score analysis after pIX protein refinement in ChAdOx1 (PDF)

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    Cited By

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    This article is cited by 3 publications.

    1. Saad Raza, Daipayan Sarkar, Leanne Jade G. Chan, Joshua Mae, Markus Sutter, Christopher J. Petzold, Cheryl A. Kerfeld, Corie Y. Ralston, Sayan Gupta, Josh V. Vermaas. Comparative Pore Structure and Dynamics for Bacterial Microcompartment Shell Protein Assemblies in Sheets or Shells. ACS Omega 2024, 9 (33) , 35503-35514. https://doi.org/10.1021/acsomega.4c02406
    2. Zakaria L. Dahmani, Ana Ligia Scott, Catherine Vénien-Bryan, David Perahia, Mauricio G.S Costa. MDFF_NM: Improved Molecular Dynamics Flexible Fitting into Cryo-EM Density Maps with a Multireplica Normal Mode-Based Search. Journal of Chemical Information and Modeling 2024, 64 (13) , 5151-5160. https://doi.org/10.1021/acs.jcim.3c02007
    3. Ludmila V. Roze, Anna Antoniak, Daipayan Sarkar, Aaron H. Liepman, Mauricio Tejera‐Nieves, Josh V. Vermaas, Berkley J. Walker. Increasing thermostability of the key photorespiratory enzyme glycerate 3‐kinase by structure‐based recombination. Plant Biotechnology Journal 2024, https://doi.org/10.1111/pbi.14508
    4. Ludmila V. Roze, Anna Antoniak, Daipayan Sarkar, Aaron H. Liepman, Mauricio Tejera-Nieves, Josh V. Vermaas, Berkley J. Walker. Advancing thermostability of the key photorespiratory enzyme glycerate 3-kinase by structure-based recombination. 2024https://doi.org/10.1101/2024.05.02.592181
    5. Saad Raza, Daipayan Sarkar, Leanne Jade G. Chan, Joshua Mae, Markus Sutter, Christopher J. Petzold, Cheryl A. Kerfeld, Corie Y. Ralston, Sayan Gupta, Josh V. Vermaas. Comparative Pore Structure and Dynamics for Bacterial Microcompartment Shell Protein Assemblies in Sheets or Shells. 2024https://doi.org/10.1101/2024.03.12.584231

    Journal of Chemical Information and Modeling

    Cite this: J. Chem. Inf. Model. 2023, 63, 18, 5834–5846
    Click to copy citationCitation copied!
    https://doi.org/10.1021/acs.jcim.3c00350
    Published September 4, 2023
    Copyright © 2023 American Chemical Society

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