Expanding the tool box for native structural biology: <sup>19</sup>F dynamic nuclear polarization with fast magic angle spinning.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 39356759.
- Also identified by DOI 10.1126/sciadv.adq3115 and PMC identifier 11446267.
- Licence recorded as CC BY-NC.
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Abstract
Obtaining atomic-level information on components in the cell is a major focus in structural biology. Elucidating specific structural and dynamic features of proteins and their interactions in the cellular context is crucial for understanding cellular processes. We introduce <sup>19</sup>F dynamic nuclear polarization (DNP) combined with fast magic-angle-spinning (MAS) nuclear magnetic resonance (NMR) spectroscopy as a powerful technique to study proteins in mammalian cells. We demonstrate our approach on the severe acute respiratory syndrome coronavirus 2 5F-Trp-N<sup>NTD</sup> protein, electroporated into human cells. DNP signal enhancements of 30- to 40-fold were observed, translating into over 1000-fold experimental time savings. High signal-to-noise ratio spectra were acquired on nanomole quantities of a protein in cells in minutes. 2D <sup>19</sup>F-<sup>19</sup>F dipolar correlation spectra with remarkable sensitivity and resolution were obtained, exhibiting <sup>19</sup>F-<sup>19</sup>F cross peaks associated with fluorine atoms as far as ~10 angstroms apart. This work paves the way for <sup>19</sup>F DNP-enhanced MAS NMR applications in cells for probing protein structure, dynamics, and ligand interactions.
Medical subject headings
- SARS-CoV-2
- Nuclear Magnetic Resonance, Biomolecular