From Angstroms to Nanometers: Measuring Interatomic Distances by Solid-State NMR
Author(s) -
A. Shcherbakov,
João MedeirosSilva,
Nhi Tran,
Martin D. Gelenter,
Mei Hong
Publication year - 2021
Publication title -
chemical reviews
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 20.528
H-Index - 700
eISSN - 1520-6890
pISSN - 0009-2665
DOI - 10.1021/acs.chemrev.1c00662
Subject(s) - chemistry , fluorine 19 nmr , nuclear magnetic resonance spectroscopy , magic angle spinning , carbon 13 nmr satellite , solid state nuclear magnetic resonance , nuclear magnetic resonance crystallography , chemical shift , nanometre , angstrom , transverse relaxation optimized spectroscopy , nmr spectra database , chemical physics , crystallography , nuclear magnetic resonance , spectral line , physics , stereochemistry , optics , astronomy
Internuclear distances represent one of the main structural constraints in molecular structure determination using solid-state NMR spectroscopy, complementing chemical shifts and orientational restraints. Although a large number of magic-angle-spinning (MAS) NMR techniques have been available for distance measurements, traditional 13 C and 15 N NMR experiments are inherently limited to distances of a few angstroms due to the low gyromagnetic ratios of these nuclei. Recent development of fast MAS triple-resonance 19 F and 1 H NMR probes has stimulated the design of MAS NMR experiments that measure distances in the 1-2 nm range with high sensitivity. This review describes the principles and applications of these multiplexed multidimensional correlation distance NMR experiments, with an emphasis on 19 F- and 1 H-based distance experiments. Representative applications of these long-distance NMR methods to biological macromolecules as well as small molecules are reviewed.
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