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Cryo-EM structure and B-factor refinement with ensemble representation
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DOI：10.1038/s41467-023-44593-1.png)
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摘要
En 中文
Cryo-EM experiments produce images of macromolecular assemblies that are combined to produce three-dimensional density maps. Typically, atomic models of the constituent molecules are fitted into these maps, followed by a density-guided refinement. We introduce TEMPy-ReFF, a method for atomic structure refinement in cryo-EM density maps. Our method represents atomic positions as components of a Gaussian mixture model, utilising their variances as B-factors, which are used to derive an ensemble description. Extensively tested on a substantial dataset of 229 cryo-EM maps from EMDB ranging in resolution from 2.1-4.9 angstrom with corresponding PDB and CERES atomic models, our results demonstrate that TEMPy-ReFF ensembles provide a superior representation of cryo-EM maps. On a single-model basis, it performs similarly to the CERES re-refinement protocol, although there are cases where it provides a better fit to the map. Furthermore, our method enables the creation of composite maps free of boundary artefacts. TEMPy-ReFF is useful for better interpretation of flexible structures, such as those involving RNA, DNA or ligands. Cryo-EM is the go-to method for visualizing large, flexible biomolecules. Here, authors introduce a new Gaussian mixture modelling method for cryo-EM modelling tasks, including refinement, composite map generation and ensemble representation.
Keyword:
UNIFIED DATA RESOURCE
ATOMIC MODELS
RESOLUTION STRUCTURE
ELECTRON-MICROSCOPY
PROTEIN STRUCTURES
VALIDATION
MAPS
MOLPROBITY
PARAMETERS
COMPLEX
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期刊
IF:
15.7
论文数:
9.4W
被引数:
91.2W
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