Ala-Korpela M, Hiltunen Y, Jokisaari J, Eskelinen S, Kiviniity K, Savolainen M J, Kesäniemi Y A
Department of Physics, University of Oulu, Finland.
NMR Biomed. 1993 May-Jun;6(3):225-33. doi: 10.1002/nbm.1940060309.
The purpose of this work was two-fold. In the first instance, 1H NMR spectra of the ultracentrifuged lipoprotein fractions (VLDL, LDL and HDL) from six volunteers with different clinical conditions were measured. The methylene regions of the experimental spectra were modelled in the frequency domain using non-linear lineshape fitting analyses. In this way the resolvable Lorentzian component structures of the methylene regions of these lipoprotein fraction spectra could be determined. Second, the lipoprotein fraction analyses were used to construct simplified component structures, which interpreted the lipoprotein fraction spectra well, and were feasible to use in the total plasma spectra analyses. The considerable overlap problem of the resonances was properly handled in this way. The NMR-based relative amounts of the lipoproteins (relative integrated intensities of the lipoprotein model signals) obtained were compared to the biochemically resolved relative molar percentages of the lipoprotein fractions and also of the lipid contents between the lipoprotein complexes. It was noticed that nearly all correlations were extremely good. Thus, it is suggested that the developed methodology could be used as a fast method to predict the relative amounts of the lipoproteins and also possibly the relative lipid contents between the major lipoprotein categories directly from the proton NMR spectrum of a total blood plasma sample. Furthermore, if internal or external reference for the integrated intensities of the proton NMR resonances were used, it should also be possible to obtain the absolute amounts of these quantities.
这项工作有两个目的。首先,测量了来自六名不同临床状况志愿者的超速离心脂蛋白组分(极低密度脂蛋白、低密度脂蛋白和高密度脂蛋白)的1H NMR谱。使用非线性线形拟合分析在频域中对实验谱的亚甲基区域进行建模。通过这种方式,可以确定这些脂蛋白组分谱亚甲基区域可分辨的洛伦兹分量结构。其次,脂蛋白组分分析用于构建简化的组分结构,该结构能很好地解释脂蛋白组分谱,并且可用于总血浆谱分析。通过这种方式,共振的大量重叠问题得到了妥善处理。将获得的基于NMR的脂蛋白相对含量(脂蛋白模型信号的相对积分强度)与通过生化方法解析的脂蛋白组分的相对摩尔百分比以及脂蛋白复合物之间的脂质含量进行比较。结果发现几乎所有的相关性都非常好。因此,有人提出所开发的方法可以用作一种快速方法,直接从全血血浆样品的质子NMR谱预测脂蛋白的相对含量以及主要脂蛋白类别之间可能的相对脂质含量。此外,如果使用质子NMR共振积分强度的内部或外部参考,也应该能够获得这些量的绝对含量。