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Restoring resolution in biological solid-state NMR under conditions of off-magic-angle spinning.
J. Phys. Chem. Lett. 6, 5040-5044 (2015)
Spin-state-selective excitation (S3E) experiments allow the selection of individual transitions in a coupled two spin system. We show that in the solid state, the dipole-dipole interaction (DD) between 15N and 1H in a 1H-15N bond and the chemical shift anisotropy (CSA) of 15N in an amide moiety mutually cancel each other for a particular multiplet component at high field, when the sample is spun off the magic angle (Arctan [√2] = 54.74°). The accuracy of the adjustment of the spinning angle is crucial in conventional experiments. We demonstrate that for S3E experiments, the requirement to spin the sample exactly at the magic angle is not mandatory. Applications of solid state NMR in narrow bore magnets will be facilitated where the adjustment of the magic angle is often difficult. The method opens new perspectives for the development of schemes to determine distances and to quantify dynamics in the solid state.
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Publication type
Article: Journal article
Document type
Scientific Article
Keywords
Chemical Shift Anisotropy ; Dipole-dipole Interaction ; Spin-state-selective Excitation
Language
english
Publication Year
2015
HGF-reported in Year
2015
e-ISSN
1948-7185
Quellenangaben
Volume: 6,
Issue: 24,
Pages: 5040-5044
Publisher
American Chemical Society (ACS)
Reviewing status
Peer reviewed
Institute(s)
Institute of Structural Biology (STB)
POF-Topic(s)
30203 - Molecular Targets and Therapies
Research field(s)
Enabling and Novel Technologies
PSP Element(s)
G-503090-001
G-503000-001
G-503000-001
PubMed ID
26641130
WOS ID
WOS:000366886000028
Scopus ID
84951985835
Erfassungsdatum
2015-12-31