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. 2019 Jun 25;60(9):1516–1534. doi: 10.1194/jlr.M092643

TABLE 3.

Relative visibility Irel of all observed signals shown in given spectral ranges

Signal T (K) Relative Visibility Irel (%)
LDL HDL2 HDL3
CH2/CH3 region (0.1–3.0 ppm) 283 14.1 34.3 55.9
293 21.9 44.4 65.2
303 36.3 53.9 73.8
313 42.4 58.4 78.6
323 45.1 61.3 82.0
Total cholesterol C-18H3 (0.62–0.78 ppm) 283 14.3 40.0 72.0
293 19.4 50.4 77.7
303 32.3 57.8 84.9
313 38.6 61.8 89.8
323 41.8 64.4 94.2
CH3 FAs (0.7–1.0 ppm) 283 21.3 35.3 51.9
293 38.1 50.0 70.1
303 64.1 63.7 79.5
313 73.1 70.1 86.9
323 76.2 73.7 91.7
Bis-allylic-methylene (2.6–2.8 ppm) 283 6.2 23.0 41.4
293 13.9 35.6 56.2
303 36.1 44.8 71.4
313 40.4 52.3 76.8
323 43.1 55.1 82.6
Choline N+(CH3)3 (3.0–3.4 ppm) 283 26.2 53.9 66.7
293 29.1 62.3 71.5
303 38.1 70.1 77.5
313 42.8 74.7 87.1
323 46.4 77.6 89.2

The relative visibilities Irel are calculated from the normalized individual peak areas in the lipoprotein spectra ILP divided by the corresponding peak areas Ilipid of the extracted lipids. The given values are the average of the two samples of the same healthy donor. The ppm values given correspond to the approximate limits of the peaks in native lipoprotein preparations. The error estimated from the two parallel estimations is about 5%. The intensity of the noncholesterol methyl groups is obtained as described in Materials and Methods. Bold type indicates the recommended experimental temperature.