Efficient in situ screening of and data collection from microcrystals in crystallization plates.
Amy J ThompsonJuan Sanchez-WeatherbyLewis J WilliamsHalina MikolajekJames SandyJonathan A R WorrallMichael A HoughPublished in: Acta crystallographica. Section D, Structural biology (2024)
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.