KAMO: towards automated data processing for microcrystals

被引:184
|
作者
Yamashita, Keitaro [1 ]
Hirata, Kunio [1 ]
Yamamoto, Masaki [1 ]
机构
[1] RIKEN, SPring Ctr 8, Sayo 6795148, Japan
关键词
automatic data processing; microcrystals; KAMO; small-wedge data sets; X-RAY CRYSTALLOGRAPHY; SERIAL; MEMBRANE; SOFTWARE; ALGORITHMS; SELECTION; CRYSTALS; PROTEINS;
D O I
10.1107/S2059798318004576
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
In protein microcrystallography, radiation damage often hampers complete and high-resolution data collection from a single crystal, even under cryogenic conditions. One promising solution is to collect small wedges of data (5-10 degrees) separately from multiple crystals. The data from these crystals can then be merged into a complete reflection-intensity set. However, data processing of multiple small-wedge data sets is challenging. Here, a new open-source data-processing pipeline, KAMO, which utilizes existing programs, including the XDS and CCP4 packages, has been developed to automate whole data-processing tasks in the case of multiple small-wedge data sets. Firstly, KAMO processes individual data sets and collates those indexed with equivalent unit-cell parameters. The space group is then chosen and any indexing ambiguity is resolved. Finally, clustering is performed, followed by merging with outlier rejections, and a report is subsequently created. Using synthetic and several real-world data sets collected from hundreds of crystals, it was demonstrated that merged structure-factor amplitudes can be obtained in a largely automated manner using KAMO, which greatly facilitated the structure analyses of challenging targets that only produced microcrystals.
引用
收藏
页码:441 / 449
页数:9
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