Nature Communications (Apr 2023)

Millisecond cryo-trapping by the spitrobot crystal plunger simplifies time-resolved crystallography

  • Pedram Mehrabi,
  • Sihyun Sung,
  • David von Stetten,
  • Andreas Prester,
  • Caitlin E. Hatton,
  • Stephan Kleine-Döpke,
  • Alexander Berkes,
  • Gargi Gore,
  • Jan-Philipp Leimkohl,
  • Hendrik Schikora,
  • Martin Kollewe,
  • Holger Rohde,
  • Matthias Wilmanns,
  • Friedjof Tellkamp,
  • Eike C. Schulz

DOI
https://doi.org/10.1038/s41467-023-37834-w
Journal volume & issue
Vol. 14, no. 1
pp. 1 – 9

Abstract

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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.