Spitrobot-2 advances time-resolved cryo-trapping crystallography to under 25 ms

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.

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Journal
Communications Chemistry
Published
2025-11-20
DOI
https://doi.org/10.1038/s42004-025-01784-9
Primary Topic
Enzyme Structure and Function
Type
article
Field-Weighted Citation Impact
0.00

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article

Spitrobot-2 advances time-resolved cryo-trapping crystallography to under 25 ms

Caitlin E. Hatton, Friedjof Tellkamp, Martin Kollewe, P. Mehrabi et al.
Communications Chemistry
Enzyme Structure and Function
article

Spitrobot-2 advances time-resolved cryo-trapping crystallography to under 25 ms

Caitlin E. Hatton, Friedjof Tellkamp, Martin Kollewe, P. Mehrabi, Jan-Philipp Leimkohl, Maria Spiliopoulou, Eike C. Schulz, Hendrik Schikora
article en

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.

Communications ChemistryVol. 8(1)
Universität Hamburg (DE), University Medical Center Hamburg-Eppendorf (DE), Hamburg Institut (Germany) (DE), Max Planck Institute for the Structure and Dynamics of Matter (DE)
Joachim Herz Stiftung, European Commission, Deutsche Forschungsgemeinschaft, Bundesministerium für Bildung und Forschung, Max-Planck-Gesellschaft
Openalex Percentile: Top 72%
Enzyme Structure and Function
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