Topf, Maya (2021) Assessment of protein-protein interfaces in cryo-EM derived assemblies. Nature Communications 12 (3399), ISSN 2041-1723.
|
Text
44467.pdf - Published Version of Record Available under License Creative Commons Attribution. Download (2MB) | Preview |
Abstract
Structures of macromolecular assemblies derived from cryo-EM maps often contain errors that become more abundant with decreasing resolution. Despite efforts in the cryo-EM community to develop metrics for map and atomistic model validation, thus far, no specific scoring metrics have been applied systematically to assess the interface between the assembly subunits. Here, we comprehensively assessed protein–protein interfaces in macromolecular assemblies derived by cryo-EM. To this end, we developed Protein Interface-score (PI-score), a density-independent machine learning-based metric, trained using the features of protein–protein interfaces in crystal structures. We evaluated 5873 interfaces in 1053 PDB-deposited cryo-EM models (including SARS-CoV-2 complexes), as well as the models submitted to CASP13 cryo-EM targets and the EM model challenge. We further inspected the interfaces associated with low-scores and found that some of those, especially in intermediate-to-low resolution (worse than 4 Å) structures, were not captured by density-based assessment scores. A combined score incorporating PI-score and fit-to-density score showed discriminatory power, allowing our method to provide a powerful complementary assessment tool for the ever-increasing number of complexes solved by cryo-EM.
Metadata
Item Type: | Article |
---|---|
School: | Birkbeck Faculties and Schools > Faculty of Science > School of Natural Sciences |
Depositing User: | Administrator |
Date Deposited: | 07 Jun 2021 10:40 |
Last Modified: | 02 Aug 2023 18:10 |
URI: | https://eprints.bbk.ac.uk/id/eprint/44467 |
Statistics
Additional statistics are available via IRStats2.