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

IUCrJ

Gilski, M.¹  Svensson, O.² 

[1]European Molecular Biology Laboratory, Grenoble Outstation, 71 Avenue des Martyrs, CS 90181, F-38042 Grenoble, France

[2]European Synchrotron Radiation Facility, 71 Avenue des Martyrs, CS 40220, F-38043 Grenoble, France

关键词: MASSIF-1;    DATA COLLECTION;    BIOLOGICAL MACROMOLECULES;    CRYSTAL MORPHOLOGY;   

DOI  :  10.1107/S2052252519008017

学科分类：数学（综合）

来源: International Union of Crystallography

【 摘 要 】

The 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 sample-location, characterization 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, the space group, the 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, 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.

【 授权许可】

CC BY