TY - JOUR
T1 - When Small becomes Too Big
T2 - Expanding the Use of In-Cell Solid-State NMR Spectroscopy
AU - Narasimhan, Siddarth
AU - Folkers, Gert E
AU - Baldus, Marc
N1 - © 2020 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.
PY - 2020/4/2
Y1 - 2020/4/2
N2 - Solution-state NMR spectroscopy has become a powerful tool to study soluble proteins in cells, provided that they tumble sufficiently fast. In addition, cryo-electron tomography (cryo-ET) has recently displayed a tremendous potential to probe structures of large proteins and assemblies in their native cellular environments. However, challenges remain to obtain atomic-level information in native cell settings for proteins that are small, disordered, or are strongly engaged in intermolecular interactions. In this Minireview, we discuss recent progress in using sensitivity enhanced solid-state NMR spectroscopy methods in the context of cellular structural biology.
AB - Solution-state NMR spectroscopy has become a powerful tool to study soluble proteins in cells, provided that they tumble sufficiently fast. In addition, cryo-electron tomography (cryo-ET) has recently displayed a tremendous potential to probe structures of large proteins and assemblies in their native cellular environments. However, challenges remain to obtain atomic-level information in native cell settings for proteins that are small, disordered, or are strongly engaged in intermolecular interactions. In this Minireview, we discuss recent progress in using sensitivity enhanced solid-state NMR spectroscopy methods in the context of cellular structural biology.
U2 - 10.1002/cplu.202000167
DO - 10.1002/cplu.202000167
M3 - Review article
C2 - 32297474
SN - 2192-6506
VL - 85
SP - 760
EP - 768
JO - ChemPlusChem
JF - ChemPlusChem
IS - 4
ER -