Departments of Molecular Genetics, Biochemistry and Chemistry, The University of Toronto, Toronto, Ontario, Canada M5S 1A8.
J Magn Reson. 2011 Jun;210(2):159-70. doi: 10.1016/j.jmr.2011.03.008. Epub 2011 Mar 8.
With the development of appropriate labeling schemes and the associated experiments that exploit them it has become possible to record high quality solution NMR spectra of supra-molecular complexes with molecular masses extending to 1MDa. One such approach involves selective (13)CH(3) methyl labeling in highly deuterated proteins using experiments that make use of a methyl-TROSY effect that significantly improves both resolution and sensitivity in spectra. The utility of this methodology has been demonstrated on a growing number of interesting particles. It seems appropriate at this juncture, therefore, to 'step back' and evaluate the role that solution NMR spectroscopy can play in what has traditionally been the domain of X-ray crystallography and more recently cryo-electron microscopy. It is argued here that solution NMR can make a critical contribution to our understanding of how dynamics regulate function in these high molecular weight systems. Several examples from work in my laboratory on the proteasome are presented as an illustration.
随着合适的标记方案的发展以及利用这些方案进行的相关实验,已经有可能记录分子量高达 1MDa 的超分子复合物的高质量溶液 NMR 谱。一种这样的方法涉及使用利用甲基-TROSY 效应的实验,对高度氘化的蛋白质进行选择性(13)CH(3)甲基标记,该效应可显著提高谱图的分辨率和灵敏度。这种方法的实用性已经在越来越多的有趣颗粒上得到了证明。因此,在这个时候,“退后一步”并评估溶液 NMR 光谱在传统上属于 X 射线晶体学和最近的冷冻电子显微镜领域中可以发挥的作用似乎是合适的。这里认为,溶液 NMR 可以对我们理解动力学如何调节这些高分子量系统中的功能做出关键贡献。作为说明,展示了我实验室在蛋白酶体上的几个工作示例。