Towards quantitative analysis of conformational landscapes: benchmarking heterogeneous reconstruction tools in cryo-EM
Laurel F. Kinman, Andrew V. Grassetti, Maria V. Carreira, Joseph H. Davis

TL;DR
This paper introduces benchmark datasets for evaluating cryo-EM tools that reconstruct protein conformational landscapes, highlighting the challenges in assigning accurate labels to particle conformations.
Contribution
The paper introduces real cryo-EM datasets with encoded ground-truth heterogeneity for benchmarking heterogeneous reconstruction tools.
Findings
Accurate per-particle conformational label assignment remains challenging for existing software pipelines.
The developed datasets have substantial potential for benchmarking and improving heterogeneous reconstruction algorithms.
Abstract
As a single-molecule approach, cryo- electron microscopy (cryo-EM) offers the possibility of reconstructing in exquisite detail the conformational landscapes occupied by dynamic protein complexes. The potential to quantitatively characterize these landscapes is particularly exciting, as it would allow us to understand how drugs, binding partners, and other experimental and environmental perturbations tune these landscapes to regulate biological function. However, quantitative analysis of conformational landscapes via cryo-EM requires both comprehensive identification of all structural states present in a sample, and high-confidence assignment of individual particles to their corresponding conformational state, two tasks that have proven challenging given the low signal-to-noise ratio of the underlying data. While there has been an emergence of statistical and machine learning - based…
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Taxonomy
TopicsPhysics of Superconductivity and Magnetism · Advanced Electron Microscopy Techniques and Applications
