The complex analysis of X-ray mesh scans for macromolecular crystallography

被引:23
作者
Melnikov, Igor [1 ]
Svensson, Olof [1 ]
Bourenkov, Gleb [2 ]
Leonard, Gordon [1 ]
Popov, Alexander [1 ]
机构
[1] European Synchrotron Radiat Facil, BP 220, F-38043 Grenoble, France
[2] European Mol Biol Lab, Hamburg Outstn, Notkestr 85, D-22607 Hamburg, Germany
来源
ACTA CRYSTALLOGRAPHICA SECTION D-STRUCTURAL BIOLOGY | 2018年 / 74卷
关键词
macromolecular crystallography; X-ray mesh scans; sample localization; data-collection strategies; MeshBest; DATA-COLLECTION; SYNCHROTRON-RADIATION; CRYSTAL DETECTION; PROTEIN CRYSTALS; ANOMALOUS SCATTERING; PIXEL DETECTOR; BEAMLINES; ESRF; DIFFRACTION; VISUALIZATION;
D O I
10.1107/S2059798318002735
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
In macromolecular crystallography, mesh (raster) scans are carried out either as part of X-ray-based crystal-centring routines or to identify positions on the sample holder from which diffraction images can be collected. Here, the methods used in MeshBest, software which automatically analyses diffraction images collected during a mesh scan and produces a two-dimensional crystal map showing estimates of the dimensions, centre positions and diffraction qualities of each crystal contained in the mesh area, are presented. Sample regions producing diffraction images resulting from the superposition of more than one crystal are also distinguished from regions with single-crystal diffraction. The applicability of the method is demonstrated using several cases.
引用
收藏
页码:355 / 365
页数:11
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