In the last two decades, solid-state
nuclear magnetic resonance
(ssNMR) spectroscopy has transformed from a spectroscopic technique
investigating small molecules and industrial polymers to a potent
tool decrypting structure and underlying dynamics of complex biological
systems, such as membrane proteins, fibrils, and assemblies, in near-physiological
environments and temperatures. This transformation can be ascribed
to improvements in hardware design, sample preparation, pulsed methods,
isotope labeling strategies, resolution, and sensitivity. The fundamental
engagement between nuclear spins and radio-frequency pulses in the
presence of a strong static magnetic field is identical between solution
and ssNMR, but the experimental procedures vastly differ because of
the absence of molecular tumbling in solids. This review discusses
routinely employed state-of-the-art static and MAS pulsed NMR methods
relevant for biological samples with rotational correlation times
exceeding 100’s of nanoseconds. Recent developments in signal
filtering approaches, proton methodologies, and multiple acquisition
techniques to boost sensitivity and speed up data acquisition at fast
MAS are also discussed. Several examples of protein structures (globular,
membrane, fibrils, and assemblies) solved with ssNMR spectroscopy
have been considered. We also discuss integrated approaches to structurally
characterize challenging biological systems and some newly emanating
subdisciplines in ssNMR spectroscopy.