Small-angle scattering for structural biology-Expanding the frontier while avoiding the pitfalls

被引:310
作者
Jacques, David A. [1 ]
Trewhella, Jill [1 ]
机构
[1] Univ Sydney, Sch Mol & Microbial Biosci, Sydney, NSW 2006, Australia
基金
澳大利亚研究理事会;
关键词
Small-angle scattering; neutron scattering; X-ray scattering; protein structure; protein complexes; structural modeling; SAXS; SANS; contrast variation; X-RAY-SCATTERING; KINASE INHIBITOR SDA; BINDING-PROTEIN-C; NEUTRON-SCATTERING; CRYSTAL-STRUCTURE; ANGSTROM RESOLUTION; RIBOSOMAL-SUBUNIT; BACILLUS-SUBTILIS; ESCHERICHIA-COLI; MOLECULAR-WEIGHT;
D O I
10.1002/pro.351
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
The last decade has seen a dramatic increase in the use of small-angle scattering for the study of biological macromolecules in solution. The drive for more complete structural characterization of proteins and their interactions, coupled with the increasing availability of instrumentation and easy-to-use software for data analysis and interpretation, is expanding the utility of the technique beyond the domain of the biophysicist and into the realm of the protein scientist. However, the absence of publication standards and the ease with which 3D models can be calculated against the inherently 1D scattering data means that an understanding of sample quality, data quality, and modeling assumptions is essential to have confidence in the results. This review is intended to provide a road map through the small-angle scattering experiment, while also providing a set of guidelines for the critical evaluation of scattering data. Examples of current best practice are given that also demonstrate the power of the technique to advance our understanding of protein structure and function.
引用
收藏
页码:642 / 657
页数:16
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