Cohen S L, Chait B T
Laboratory for Mass Spectrometry and Gaseous Ion Chemistry, Rockefeller University, New York, NY 10021, USA.
Annu Rev Biophys Biomol Struct. 2001;30:67-85. doi: 10.1146/annurev.biophys.30.1.67.
Atomic resolution structure determinations of proteins by X-ray crystallography are formidable multidisciplinary undertakings, requiring protein construct design, expression and purification, crystallization trials, phase determination, and model building. Modern mass spectrometric methods can greatly facilitate these obligate tasks. Thus, mass spectrometry can be used to verify that the desired protein construct has been correctly expressed, to define compact domains in the target protein, to assess the components contained within the protein crystals, and to screen for successful incorporation of seleno-methionine and other heavy metal reagents used for phasing. In addition, mass spectrometry can be used to address issues of modeling, topology, and side-chain proximity. Here, we demonstrate how rational use of mass spectrometry assists and expedites high resolution X-ray structure determination through each stage of the process of protein crystallography.
通过X射线晶体学测定蛋白质的原子分辨率结构是一项艰巨的多学科任务,需要进行蛋白质构建体设计、表达与纯化、结晶试验、相位确定以及模型构建。现代质谱方法能够极大地促进这些必要任务的完成。因此,质谱可用于验证所需的蛋白质构建体是否已正确表达,确定目标蛋白质中的紧密结构域,评估蛋白质晶体中所含的成分,以及筛选用于相位确定的硒代甲硫氨酸和其他重金属试剂是否成功掺入。此外,质谱还可用于解决建模、拓扑结构和侧链接近度等问题。在此,我们展示了合理运用质谱如何在蛋白质晶体学过程的每个阶段辅助并加速高分辨率X射线结构的测定。