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

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.

Bibliographical data

Original languageEnglish
ISSN2041-1723
DOIs
Publication statusPublished - 25.04.2023

Comment Deanary

© 2023. The Author(s).

PubMed 37185266