Progress in rational methods of cryoprotection in macromolecular crystallography

被引:37
作者
Alcorn, Thomas [1 ]
Juers, Douglas H. [1 ,2 ]
机构
[1] Whitman Coll, Program Biochem Biophys & Mol Biol, Walla Walla, WA 99362 USA
[2] Whitman Coll, Dept Phys, Walla Walla, WA 99362 USA
来源
ACTA CRYSTALLOGRAPHICA SECTION D-STRUCTURAL BIOLOGY | 2010年 / 66卷
关键词
X-RAY-DIFFRACTION; PROTEIN CRYSTALS; RADIATION-DAMAGE; THERMAL-EXPANSION; BIOLOGICAL MACROMOLECULES; CRYSTALLIZATION SOLUTIONS; CRYOGENIC TEMPERATURES; ROOM-TEMPERATURE; INSULIN CRYSTALS; CRYOCRYSTALLOGRAPHY;
D O I
10.1107/S090744490903995X
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Cryogenic cooling of macromolecular crystals is commonly used for X-ray data collection both to reduce crystal damage from radiation and to gather functional information by cryogenically trapping intermediates. However, the cooling process can damage the crystals. Limiting cooling-induced crystal damage often requires cryoprotection strategies, which can involve substantial screening of solution conditions and cooling protocols. Here, recent developments directed towards rational methods for cryoprotection are described. Crystal damage is described in the context of the temperature response of the crystal as a thermodynamic system. As such, the internal and external parts of the crystal typically have different cryoprotection requirements. A key physical parameter, the thermal contraction, of 26 different cryoprotective solutions was measured between 294 and 72 K. The range of contractions was 2 -13%, with the more polar cryosolutions contracting less. The potential uses of these results in the development of cryocooling conditions, as well as recent developments in determining minimum cryosolution soaking times, are discussed.
引用
收藏
页码:366 / 373
页数:8
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