Achieving a Good Crystal System for Crystallographic X-Ray Fragment Screening

被引:30
作者
Collins, Patrick M. [1 ]
Douangamath, Alice [1 ]
Talon, Romain [1 ]
Dias, Alexandre [1 ]
Brandao-Neto, Jose [1 ]
Krojer, Tobias [2 ]
von Delft, Frank [1 ,2 ,3 ]
机构
[1] Diamond Light Source, Harwell Sci & Innovat Campus, Didcot, Oxon, England
[2] Univ Oxford, Nuffield Dept Med, Struct Genom Consortium, Oxford, England
[3] Univ Johannesburg, Dept Biochem, Aukland Pk, South Africa
来源
MODERN APPROACHES IN DRUG DISCOVERY | 2018年 / 610卷
关键词
PROTEIN CRYSTALLIZATION;
D O I
10.1016/bs.mie.2018.09.027
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The XChem facility at Diamond Light Source offers fragment screening by X-ray crystallography as a general access user program. The main advantage of X-ray crystallography as a primary fragment screen is that it yields directly the location and pose of the fragment hits, whether within pockets of interest or merely on surface sites: this is the key information for structure-based design and for enabling synthesis of follow-up molecules. Extensive streamlining of the screening experiment at XChem has engendered a very active user program that is generating large amounts of data: in 2017, 36 academic and industry groups generated 35,000 datasets of uniquely soaked crystals. It has also generated a large number of learnings concerning the main remaining bottleneck, namely, obtaining a suitable crystal system that will support a successful fragment screen. Here we discuss the practicalities of generating screen-ready crystals that have useful electron density maps, and how to ensure they will be successfully reproduced and usable at a facility outside the home lab.
引用
收藏
页码:251 / 264
页数:14
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