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. Author manuscript; available in PMC: 2022 Apr 5.
Published in final edited form as: Methods Enzymol. 2018 Sep 18;615:373–406. doi: 10.1016/bs.mie.2018.08.023

Figure 1:

Figure 1:

Dynamic nuclear polarization enhances NMR signals in cellular environments. A) One dimensional 13C{1H} CP spectra both with (blue) and without DNP enhancement (red). DNP NMR results in large signal enhancements (ε) for samples of per-deuterated cellular lysates in a 60:30:10 mixtures of d8-glycerol:D2O:H2O and 10 mM AMUPol at 600 MHz/385 GHz with ω/2π = 12.5 kHz and a sample temperature of 100 K. Spectroscopic selection for the small amount of uniformly isotopically labeled exogenous prepared protein that was added to the cellular lysate mixture reveals that the amyloid cores of this protein have similar conformations (purple line), the intrinsically disordered region (red line) has a very different chemical environment in (B) purified samples than it does in (C) in biological environments.