8BK8
Cryo-EM structure of beta-galactosidase at 2.9 A resolution plunged 205 ms after mixing with apoferritin
Summary for 8BK8
Entry DOI | 10.2210/pdb8bk8/pdb |
EMDB information | 16092 |
Descriptor | Beta-galactosidase (1 entity in total) |
Functional Keywords | glycosyl hydrolase, hydrolase |
Biological source | Escherichia coli |
Total number of polymer chains | 4 |
Total formula weight | 469953.50 |
Authors | Torino, S.,Dhurandhar, M.,Efremov, R. (deposition date: 2022-11-08, release date: 2023-08-09, Last modification date: 2023-09-13) |
Primary citation | Torino, S.,Dhurandhar, M.,Stroobants, A.,Claessens, R.,Efremov, R.G. Time-resolved cryo-EM using a combination of droplet microfluidics with on-demand jetting. Nat.Methods, 20:1400-1408, 2023 Cited by PubMed Abstract: Single-particle cryogenic electron microscopy (cryo-EM) allows reconstruction of high-resolution structures of proteins in different conformations. Protein function often involves transient functional conformations, which can be resolved using time-resolved cryo-EM (trEM). In trEM, reactions are arrested after a defined delay time by rapid vitrification of protein solution on the EM grid. Despite the increasing interest in trEM among the cryo-EM community, making trEM samples with a time resolution below 100 ms remains challenging. Here we report the design and the realization of a time-resolved cryo-plunger that combines a droplet-based microfluidic mixer with a laser-induced generator of microjets that allows rapid reaction initiation and plunge-freezing of cryo-EM grids. Using this approach, a time resolution of 5 ms was achieved and the protein density map was reconstructed to a resolution of 2.1 Å. trEM experiments on GroEL:GroES chaperonin complex resolved the kinetics of the complex formation and visualized putative short-lived conformations of GroEL-ATP complex. PubMed: 37592181DOI: 10.1038/s41592-023-01967-z PDB entries with the same primary citation |
Experimental method | ELECTRON MICROSCOPY (2.9 Å) |
Structure validation
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