Efficient in situ screening of and data collection from microcrystals in crystallization plates

Acta Crystallogr D Struct Biol. 2024 Apr 1;80(Pt 4):279-288. doi: 10.1107/S2059798324001955. Epub 2024 Mar 15.

Abstract

A considerable bottleneck in serial crystallography at XFEL and synchrotron sources is the efficient production of large quantities of homogenous, well diffracting microcrystals. Efficient high-throughput screening of batch-grown microcrystals and the determination of ground-state structures from different conditions is thus of considerable value in the early stages of a project. Here, a highly sample-efficient methodology to measure serial crystallography data from microcrystals by raster scanning within standard in situ 96-well crystallization plates is described. Structures were determined from very small quantities of microcrystal suspension and the results were compared with those from other sample-delivery methods. The analysis of a two-dimensional batch crystallization screen using this method is also described as a useful guide for further optimization and the selection of appropriate conditions for scaling up microcrystallization.

Keywords: in situ data collection; microcrystals; peroxidase; radiation damage; serial crystallography.

MeSH terms

  • Crystallization / methods
  • Crystallography, X-Ray
  • Data Collection
  • Synchrotrons*