The protein as a variable in protein crystallization

被引:134
|
作者
Dale, GE [1 ]
Oefner, C [1 ]
D'Arcy, A [1 ]
机构
[1] Morphochem AG, CH-4058 Basel, Switzerland
关键词
crystallization; protein modification; mutagenesis; light scattering; truncation; fusion proteins;
D O I
10.1016/S1047-8477(03)00041-8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Strategies for growing protein crystals have for many years been essentially empirical, the protein, once purified to a certain homogeneity, being mixed with a selection of crystallization agents selected in a more or less trial-and-error fashion. Screening for the correct conditions has been made easier through automation and by the introduction of commercially available crystallization kits. Many parameters can be changed in these experiments, such as temperature, pH, and ionic strength, but perhaps the most important variable has been ignored, namely the protein. The crystallization properties of a protein vary greatly: some crystallize readily, whereas others have proven extremely difficult or even impossible to obtain in a crystalline state. The possibility of altering the intrinsic characteristics of a protein for crystallization has become a feasible strategy. Some historical perspectives and advances in this area will be reviewed. (C) 2003 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:88 / 97
页数:10
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