Adaptive Ensemble Refinement of Protein Structures in High Resolution Electron Microscopy Density Maps with Radical Augmented Molecular Dynamics Flexible FittingClick to copy article linkArticle link copied!
- Daipayan Sarkar*Daipayan Sarkar*Email: [email protected]MSU-DOE Plant Research Laboratory, East Lansing, Michigan 48824, United StatesSchool of Molecular Sciences, Arizona State University, Tempe, Arizona 85281, United StatesMore by Daipayan Sarkar
- Hyungro LeeHyungro LeePacific Northwest National Laboratory, Richland, Washington 99354, United StatesElectrical & Computer Engineering, Rutgers University, New Brunswick, New Jersey 08854, United StatesMore by Hyungro Lee
- John W. VantJohn W. VantSchool of Molecular Sciences, Arizona State University, Tempe, Arizona 85281, United StatesMore by John W. Vant
- Matteo TurilliMatteo TurilliElectrical & Computer Engineering, Rutgers University, New Brunswick, New Jersey 08854, United StatesComputational Science Initiative, Brookhaven National Laboratory, Upton, New York 11973, United StatesMore by Matteo Turilli
- Josh V. VermaasJosh V. VermaasMSU-DOE Plant Research Laboratory, East Lansing, Michigan 48824, United StatesMore by Josh V. Vermaas
- Shantenu Jha*Shantenu Jha*Email: [email protected]Electrical & Computer Engineering, Rutgers University, New Brunswick, New Jersey 08854, United StatesComputational Science Initiative, Brookhaven National Laboratory, Upton, New York 11973, United StatesMore by Shantenu Jha
- Abhishek Singharoy*Abhishek Singharoy*Email: [email protected]School of Molecular Sciences, Arizona State University, Tempe, Arizona 85281, United StatesMore by Abhishek Singharoy
Abstract
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.
Cited By
This article is cited by 3 publications.
- 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
- 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
- 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
- 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
- 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
Article Views are the COUNTER-compliant sum of full text article downloads since November 2008 (both PDF and HTML) across all institutions and individuals. These metrics are regularly updated to reflect usage leading up to the last few days.
Citations are the number of other articles citing this article, calculated by Crossref and updated daily. Find more information about Crossref citation counts.
The Altmetric Attention Score is a quantitative measure of the attention that a research article has received online. Clicking on the donut icon will load a page at altmetric.com with additional details about the score and the social media presence for the given article. Find more information on the Altmetric Attention Score and how the score is calculated.