Kerfah Rime, Plevin Michael J, Sounier Remy, Gans Pierre, Boisbouvier Jerome
University Grenoble Alpes, Institut de Biologie Structurale (IBS), F-38044 Grenoble, France; CNRS, F-38044 Grenoble, France; CEA, DSV, F-38044 Grenoble, France.
Department of Biology, University of York, York YO10 5DD, UK.
Curr Opin Struct Biol. 2015 Jun;32:113-22. doi: 10.1016/j.sbi.2015.03.009. Epub 2015 Apr 13.
Nuclear magnetic resonance (NMR) spectroscopy is a uniquely powerful tool for studying the structure, dynamics and interactions of biomolecules at atomic resolution. In the past 15 years, the development of new isotopic labeling strategies has opened the possibility of exploiting NMR spectroscopy in the study of supra-molecular complexes with molecular weights of up to 1MDa. At the core of these isotopic labeling developments is the specific introduction of [(1)H,(13)C]-labeled methyl probes into perdeuterated proteins. Here, we describe the evolution of these approaches and discuss their impact on structural and biological studies. The relevant protocols are succinctly reviewed for single and combinatorial isotopic-labeling of methyl-containing residues, and examples of applications on challenging biological systems, including high molecular weight and membrane proteins, are presented.
核磁共振(NMR)光谱是一种独特而强大的工具,可在原子分辨率下研究生物分子的结构、动力学和相互作用。在过去15年中,新的同位素标记策略的发展为利用NMR光谱研究分子量高达1MDa的超分子复合物开辟了可能性。这些同位素标记发展的核心是将[(1)H,(13)C]标记的甲基探针特异性引入全氘代蛋白质中。在此,我们描述了这些方法的演变,并讨论了它们对结构和生物学研究的影响。对含甲基残基的单同位素标记和组合同位素标记的相关方案进行了简要综述,并展示了在具有挑战性的生物系统(包括高分子量和膜蛋白)上的应用实例。