EMD-22757

Single-particle
3.3 Å
EMD-22757 Deposition: 29/09/2020
Map released: 02/12/2020
Last modified: 06/03/2024
Overview 3D View Sample Experiment Validation Volume Browser Additional data Links
Overview 3D View Sample Experiment Validation Volume Browser Additional data Links

EMD-22757

Aldolase, rabbit muscle (beam-tilt refinement x3)

EMD-22757

Single-particle
3.3 Å
EMD-22757 Deposition: 29/09/2020
Map released: 02/12/2020
Last modified: 06/03/2024
Overview 3D View Sample Experiment Validation Volume Browser Additional data Links
Sample Organism: Oryctolagus cuniculus
Sample: Homotetramer of aldolase
Fitted models: 7ka3 (Avg. Q-score: 0.515)
Raw data: EMPIAR-10519

Deposition Authors: Kearns SK, Cash JN
High-resolution cryo-EM using beam-image shift at 200 keV.
Cash JN , Kearns S , Li Y, Cianfrocco MA
(2020) IUCrJ , 7 , 1179 - 1187
PUBMED: 33209328
DOI: doi:10.1107/S2052252520013482
ISSN: 2052-2525
Abstract:
Recent advances in single-particle cryo-electron microscopy (cryo-EM) data collection utilize beam-image shift to improve throughput. Despite implementation on 300 keV cryo-EM instruments, it remains unknown how well beam-image-shift data collection affects data quality on 200 keV instruments and the extent to which aberrations can be computationally corrected. To test this, a cryo-EM data set for aldolase was collected at 200 keV using beam-image shift and analyzed. This analysis shows that the instrument beam tilt and particle motion initially limited the resolution to 4.9 Å. After particle polishing and iterative rounds of aberration correction in RELION, a 2.8 Å resolution structure could be obtained. This analysis demonstrates that software correction of microscope aberrations can provide a significant improvement in resolution at 200 keV.