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bioRxiv · 10.1101/558023

A comparative anatomy of protein crystals: lessons from the automatic processing of 56,000 samples

Svensson, O.·Gilski, M.·Nurizzo, D.·Bowler, M. W.
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Abstract

SynopsisThe automatic processing of over 56,000 crystals by the autonomous ESRF beamline MASSIF-1 has provided a data set of crystal characteristics and properties that allows many theoretical proposals and assumptions to be evaluated experimentally. AbstractThe fully automatic processing of crystals of macromolecules has presented a unique opportunity to gather information on the samples that is not usually recorded. This has proved invaluable in improving the sample location, characterisation and data collection algorithms. After operating for four years, MASSIF-1 has now processed over 56,000 samples, gathering information at each stage, from the volume of the crystal to the unit cell dimensions, space group, quality of the data collected and the reasoning behind the decisions made in data collection. This provides an unprecedented opportunity to analyse these data together, providing a detailed landscape of macromolecular crystals and intimate details of their contents and, importantly, how the two are related. The data show that mosaic spread is unrelated to the size or shape of crystals and demonstrate experimentally that diffraction intensities scale in proportion to crystal volume and molecular weight. It is also shown that crystal volume scales inversely with molecular weight. The results set the scene for the development of X-ray crystallography in a changing environment for structural biology.

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Svensson, O., Gilski, M., Nurizzo, D., Bowler, M. W.. 2019-02-22. A comparative anatomy of protein crystals: lessons from the automatic processing of 56,000 samples. https://doi.org/10.1101/558023

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