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. 2014 Mar 28;136(17):6313–6325. doi: 10.1021/ja4126092

Figure 1.

Figure 1

Spectroscopic characterization of hβ2m and ΔN6 fibrils. Negative stain electron micrographs (EM) of (a) hβ2m and (b) ΔN6 fibrils (scale bar 100 nm) and their MAS NMR spectra of (c–e) 13C–13C and (f–h) 13C–15N correlations. (c–e) One-bond RFDR spectra of U–13C,15N-hβ2m (blue) and U–13C,15N-ΔN6 (red). The cross sections of S52 are shown in (e) to illustrate the peak intensity and line width. (f–h) One-bond ZF TEDOR spectra of 1,3-hβ2m (blue) and 1,3-ΔN6 (red). (c–e) and (f–h) were acquired at 900 and 800 MHz 1H frequencies, respectively. Assignments in spectra are residue-specific and are based on 2D and 3D experiments.