bims-lances Biomed News
on Landscapes from Cryo-EM and Simulations
Issue of 2024‒06‒16
four papers selected by
James M. Krieger, National Centre for Biotechnology



  1. bioRxiv. 2024 Jun 02. pii: 2024.05.30.596729. [Epub ahead of print]
      Proteins and other biomolecules form dynamic macromolecular machines that are tightly orchestrated to move, bind, and perform chemistry. Cryo-electron microscopy (cryo-EM) can access the intrinsic heterogeneity of these complexes and is therefore a key tool for understanding mechanism and function. However, 3D reconstruction of the resulting imaging data presents a challenging computational problem, especially without any starting information, a setting termed ab initio reconstruction. Here, we introduce a method, DRGN-AI, for ab initio heterogeneous cryo-EM reconstruction. With a two-step hybrid approach combining search and gradient-based optimization, DRGN-AI can reconstruct dynamic protein complexes from scratch without input poses or initial models. Using DRGN-AI, we reconstruct the compositional and conformational variability contained in a variety of benchmark datasets, process an unfiltered dataset of the DSL1/SNARE complex fully ab initio, and reveal a new "supercomplex" state of the human erythrocyte ankyrin-1 complex. With this expressive and scalable model for structure determination, we hope to unlock the full potential of cryo-EM as a high-throughput tool for structural biology and discovery.
    DOI:  https://doi.org/10.1101/2024.05.30.596729
  2. Biotechniques. 2024 Jun 12. 1-6
      Cryo-EM has been a key technique in our understanding of biomolecular structures. Now, machine learning techniques are being used to put these structures in motion, revealing dynamic interactions and processes happening on a molecular and cellular level.[Formula: see text].
    Keywords:  3DFlex; biomolecules; cryo-EM; machine learning
    DOI:  https://doi.org/10.1080/07366205.2024.2355771
  3. bioRxiv. 2024 Jun 02. pii: 2024.05.30.596698. [Epub ahead of print]
      The Tropomyosin 1 isoform I/C C-terminal domain (Tm1-LC) fibril structure is studied jointly with cryogenic electron microscopy (cryo-EM) and solid state nuclear magnetic resonance (NMR). This study demonstrates the complementary nature of these two structural biology techniques. Chemical shift assignments from solid state NMR are used to determine the secondary structure at the level of individual amino acids, which is faithfully seen in cryo-EM reconstructions. Additionally, solid state NMR demonstrates that the region not observed in the reconstructed cryo-EM density is primarily in a highly mobile random coil conformation rather than adopting multiple rigid conformations. Overall, this study illustrates the benefit of investigations combining cryo-EM and solid state NMR to investigate protein fibril structure.
    Keywords:  Cryogenic electron microscopy; protein fibril; protein structure; solid state nuclear magnetic resonance
    DOI:  https://doi.org/10.1101/2024.05.30.596698
  4. ArXiv. 2024 May 28. pii: arXiv:2405.18532v1. [Epub ahead of print]
      To quantify how well theoretical predictions of structural ensembles agree with experimental measurements, we depend on the accuracy of forward models. These models are computational frameworks that generate observable quantities from molecular configurations based on empirical relationships linking specific molecular properties to experimental measurements. Bayesian Inference of Conformational Populations (BICePs) is a reweighting algorithm that reconciles simulated ensembles with ensemble-averaged experimental observations, even when such observations are sparse and/or noisy. This is achieved by sampling the posterior distribution of conformational populations under experimental restraints as well as sampling the posterior distribution of uncertainties due to random and systematic error. In this study, we enhance the algorithm for the refinement of empirical forward model (FM) parameters. We introduce and evaluate two novel methods for optimizing FM parameters. The first method treats FM parameters as nuisance parameters, integrating over them in the full posterior distribution. The second method employs variational minimization of a quantity called the BICePs score that reports the free energy of "turning on" the experimental restraints. This technique, coupled with improved likelihood functions for handling experimental outliers, facilitates force field validation and optimization, as illustrated in recent studies (Raddi et al. 2023, 2024). Using this approach, we refine parameters that modulate the Karplus relation, crucial for accurate predictions of J -coupling constants based on dihedral angles (ϕ) between interacting nuclei. We validate this approach first with a toy model system, and then for human ubiquitin, predicting six sets of Karplus parameters for JHNHα3 , JHαC'3 , JHNCβ3 , JHNC'3 , JC'Cβ3 , JC'C'3 . This approach, which does not rely on any predetermined parameterization, enhances predictive accuracy and can be used for many applications.