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9R46

Spitrobot-2 advances time-resolvedcryo-trapping crystallography to under 25 ms: Xylose isomerase bound with glucose (25 ms soaking)

Summary for 9R46
Entry DOI10.2210/pdb9r46/pdb
DescriptorXylose isomerase, MAGNESIUM ION, MANGANESE (II) ION, ... (5 entities in total)
Functional Keywordsxylose isomerase, glucose, spitrobot-2, isomerase
Biological sourceStreptomyces rubiginosus
Total number of polymer chains1
Total formula weight43542.70
Authors
Hatton, C.E.,Spiliopoulou, M.,Schulz, E.C.,Mehrabi, P. (deposition date: 2025-05-07, release date: 2025-12-03)
Primary citationSpiliopoulou, M.,Hatton, C.E.,Kollewe, M.,Leimkohl, J.P.,Schikora, H.,Tellkamp, F.,Mehrabi, P.,Schulz, E.C.
Spitrobot-2 advances time-resolved cryo-trapping crystallography to under 25 ms.
Commun Chem, 8:363-363, 2025
Cited by
PubMed Abstract: We previously introduced the spitrobot, a protein crystal plunging system that enables reaction quenching via cryo-trapping with a time resolution in the millisecond range. Here we present the next generation, spitrobot-2, as an integrated benchtop device. User-friendliness has been improved by semi-automatic sample exchange. Moreover, a fully automated shutter shields the liquid nitrogen from the humidified environment, improving sample integrity. Most importantly, the cryo-trapping delay time has been reduced to 23 ms, making spitrobot-2 twice as fast as the previous generation. This further expands the number of target systems that can be addressed by cryo-trapping time-resolved crystallography. Using 12 crystal structures of three independent model systems, we demonstrate successful cryo-trapping via observation of conformational changes and ligand binding within 25 ms. These improvements increase the convenient access to cryo-trapping, time-resolved X-ray crystallography empowering the MX community with efficient tools to advance research in structural biology.
PubMed: 41266557
DOI: 10.1038/s42004-025-01784-9
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.1 Å)
Structure validation

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