Department of Chemistry and Francis Bitter Magnet Laboratory, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139; email:
Annu Rev Biochem. 2015;84:465-97. doi: 10.1146/annurev-biochem-060614-034206. Epub 2015 Mar 30.
Magic angle spinning (MAS) NMR studies of amyloid and membrane proteins and large macromolecular complexes are an important new approach to structural biology. However, the applicability of these experiments, which are based on (13)C- and (15)N-detected spectra, would be enhanced if the sensitivity were improved. Here we discuss two advances that address this problem: high-frequency dynamic nuclear polarization (DNP) and (1)H-detected MAS techniques. DNP is a sensitivity enhancement technique that transfers the high polarization of exogenous unpaired electrons to nuclear spins via microwave irradiation of electron-nuclear transitions. DNP boosts NMR signal intensities by factors of 10(2) to 10(3), thereby overcoming NMR's inherent low sensitivity. Alternatively, it permits structural investigations at the nanomolar scale. In addition, (1)H detection is feasible primarily because of the development of MAS rotors that spin at frequencies of 40 to 60 kHz or higher and the preparation of extensively (2)H-labeled proteins.
魔角旋转(MAS)NMR 研究淀粉样蛋白和膜蛋白以及大型大分子复合物是结构生物学的一个重要新方法。然而,如果这些基于 (13)C 和 (15)N 检测光谱的实验的灵敏度得到提高,它们的适用性将会增强。本文讨论了两种解决该问题的进展:高频动态核极化(DNP)和 (1)H 检测 MAS 技术。DNP 是一种灵敏度增强技术,它通过微波辐照电子-核跃迁将外源不成对电子的高极化转移到核自旋。DNP 通过将 NMR 信号强度提高 10(2)到 10(3)倍,从而克服了 NMR 固有的低灵敏度。或者,它可以允许在纳摩尔范围内进行结构研究。此外,(1)H 检测主要是由于 MAS 转子的发展成为可能,其旋转频率为 40 到 60 kHz 或更高,以及广泛 (2)H 标记的蛋白质的制备。