Protein crystallization: Specific phenomena and general insights on crystallization kinetics

被引:3
|
作者
Rosenberger, F [1 ]
机构
[1] Univ Alabama, Ctr Micrograv & Mat Res, Huntsville, AL 35899 USA
来源
THEORETICAL AND TECHNOLOGICAL ASPECTS OF CRYSTAL GROWTH | 1998年 / 276-2卷
关键词
protein purity; protein crystallization; liquid-liquid phase separation; gelation; morphological instability; macrostep formation; step bunching; macrostep cascading; striations; growth sector boundaries; dislocations; growth kinetics; step kinetics; numerical simulation;
D O I
10.4028/www.scientific.net/MSF.276-277.241
中图分类号
O7 [晶体学];
学科分类号
0702 ; 070205 ; 0703 ; 080501 ;
摘要
Experimental and simulation studies of the nucleation and growth kinetics of proteins have revealed phenomena that are specific for macromolecular crystallization, and others that provide a more detailed understanding of solution crystallization in general. The more specific phenomena, which include metastable liquid-liquid phase separations and gelation prior to solid nucleation, are due to the small ratio of the intermolecular interaction-range to the size of molecules involved. The apparently more generally applicable mechanisms include the cascade-like formation of macrosteps, as an intrinsic morphological instability that roots in the coupled bulk transport and nonlinear interface kinetics in systems with mixed growth rate control. Analyses of this nonlinear response provide (a) criteria for the choice of bulk transport conditions to minimize structural defect formation, and (b) indications that the "slow" protein crystallization kinetics stems from the mutual retardation of growth steps.
引用
收藏
页码:241 / 256
页数:16
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