Gentle, fast and effective crystal soaking by acoustic dispensing

被引:61
作者
Collins, Patrick M. [1 ]
Ng, Jia Tsing [2 ]
Talon, Romain [2 ]
Nekrosiute, Karolina [1 ,2 ]
Krojer, Tobias
Douangamath, Alice [1 ]
Brandao-Neto, Jose [1 ]
Wright, Nathan [2 ]
Pearce, Nicholas M. [2 ]
von Delft, Frank [1 ,2 ,3 ]
机构
[1] Diamond Light Source, Harwell Sci & Innovat Campus, Didcot OX11 0DF, Oxon, England
[2] Univ Oxford, SGC, Oxford OX3 9DQ, England
[3] Univ Johannesburg, Dept Biochem, Aukland Pk, ZA-2006 Johannesburg, South Africa
来源
ACTA CRYSTALLOGRAPHICA SECTION D-STRUCTURAL BIOLOGY | 2017年 / 73卷
基金
英国惠康基金; 加拿大创新基金会;
关键词
fragment screening; crystal soaking; acoustic droplet ejection; Diamond Light Source I04-1; Structural Genomics Consortium; XChem; PROTEIN-LIGAND COMPLEXES; CRYSTALLIZATION DROPLETS; DRUG DISCOVERY; CRYSTALLOGRAPHY; LIBRARIES; COCRYSTALLIZATION; MICROMESHES; DIFFRACTION; REFINEMENT; EJECTION;
D O I
10.1107/S205979831700331X
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The steady expansion in the capacity of modern beamlines for high-throughput data collection, enabled by increasing X-ray brightness, capacity of robotics and detector speeds, has pushed the bottleneck upstream towards sample preparation. Even in ligand-binding studies using crystal soaking, the experiment best able to exploit beamline capacity, a primary limitation is the need for gentle and nontrivial soaking regimens such as stepwise concentration increases, even for robust and well characterized crystals. Here, the use of acoustic droplet ejection for the soaking of protein crystals with small molecules is described, and it is shown that it is both gentle on crystals and allows very high throughput, with 1000 unique soaks easily performed in under 10 min. In addition to having very low compound consumption (tens of nanolitres per sample), the positional precision of acoustic droplet ejection enables the targeted placement of the compound/solvent away from crystals and towards drop edges, allowing gradual diffusion of solvent across the drop. This ensures both an improvement in the reproducibility of X-ray diffraction and increased solvent tolerance of the crystals, thus enabling higher effective compoundsoaking concentrations. The technique is detailed here with examples from the protein target JMJD2D, a histone lysine demethylase with roles in cancer and the focus of active structure-based drug-design efforts.
引用
收藏
页码:246 / 255
页数:10
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