Dynamic Nuclear Polarization Nuclear Magnetic Resonance in Human Cells Using Fluorescent Polarizing Agents

被引:56
作者
Albert, Brice J. [1 ]
Gao, Chukun [1 ]
Sesti, Erika L. [1 ]
Saliba, Edward P. [1 ]
Alaniva, Nicholas [1 ]
Scott, Faith J. [1 ]
Sigurdsson, Snorri Th [2 ]
Barnes, Alexander B. [1 ]
机构
[1] Washington Univ, Dept Chem, One Brookings Dr, St Louis, MO 63130 USA
[2] Univ Iceland, Sci Inst, Dept Chem, Dunhaga 3, IS-107 Reykjavik, Iceland
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
SOLID-STATE NMR; PROTEIN-STRUCTURE DETERMINATION; ANGLE-SPINNING NMR; ALPHA-SYNUCLEIN; LIVING CELLS; SPECTROSCOPY; RESOLUTION; FREQUENCY; TAT; MITOCHONDRIA;
D O I
10.1021/acs.biochem.8b00257
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Solid state nuclear magnetic resonance (NMR) enables atomic-resolution characterization of the molecular structure and dynamics within complex heterogeneous samples, but it is typically insensitive. Dynamic nuclear polarization (DNP) increases the NMR signal intensity by orders of magnitude and can be performed in combination with magic angle spinning (MAS) for sensitive, high-resolution spectroscopy. Here we report MAS DNP experiments, for the first time, within intact human cells with >40-fold DNP enhancement and a sample temperature of <6 K. In addition to cryogenic MAS results at <6 K, we also show in-cell DNP enhancements of 57-fold at 90 K. In-cell DNP is demonstrated using biradicals and sterically shielded monoradicals as polarizing agents. A novel trimodal polarizing agent is introduced for DNP, which contains a nitroxide biradical, a targeting peptide for cell penetration, and a fluorophore for subcellular localization with confocal microscopy. The fluorescent polarizing agent provides in-cell DNP enhancements of 63-fold at a concentration of 2.7 mM. These experiments pave the way for structural characterization of biomolecules in an endogenous cellular context.
引用
收藏
页码:4741 / 4746
页数:6
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