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8AWY

Millisecond cryo-trapping by the spitrobot crystal plunger, Serial measurement Xylose Isomerase with 2,3-butanediol at 50ms

Summary for 8AWY
Entry DOI10.2210/pdb8awy/pdb
DescriptorXylose isomerase, MAGNESIUM ION, Meso-2,3-Butanediol, ... (4 entities in total)
Functional Keywordsxylose isomerase, glucose isomerase, humidity serial measurement, time-resolved crystallography, isomerase
Biological sourceStreptomyces rubiginosus
Total number of polymer chains1
Total formula weight43446.33
Authors
Primary citationMehrabi, P.,Sung, S.,von Stetten, D.,Prester, A.,Hatton, C.E.,Kleine-Dopke, S.,Berkes, A.,Gore, G.,Leimkohl, J.P.,Schikora, H.,Kollewe, M.,Rohde, H.,Wilmanns, M.,Tellkamp, F.,Schulz, E.C.
Millisecond cryo-trapping by the spitrobot crystal plunger simplifies time-resolved crystallography.
Nat Commun, 14:2365-2365, 2023
Cited by
PubMed Abstract: We introduce the spitrobot, a protein crystal plunger, enabling reaction quenching via cryo-trapping with a time-resolution in the millisecond range. Protein crystals are mounted on canonical micromeshes on an electropneumatic piston, where the crystals are kept in a humidity and temperature-controlled environment, then reactions are initiated via the liquid application method (LAMA) and plunging into liquid nitrogen is initiated after an electronically set delay time to cryo-trap intermediate states. High-magnification images are automatically recorded before and after droplet deposition, prior to plunging. The SPINE-standard sample holder is directly plunged into a storage puck, enabling compatibility with high-throughput infrastructure. Here we demonstrate binding of glucose and 2,3-butanediol in microcrystals of xylose isomerase, and of avibactam and ampicillin in microcrystals of the extended spectrum beta-lactamase CTX-M-14. We also trap reaction intermediates and conformational changes in macroscopic crystals of tryptophan synthase to demonstrate that the spitrobot enables insight into catalytic events.
PubMed: 37185266
DOI: 10.1038/s41467-023-37834-w
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.6 Å)
Structure validation

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