Department of Chemistry, University of Coimbra, 3004-535 Coimbra, Portugal.
Anal Biochem. 2012 Aug 1;427(1):41-8. doi: 10.1016/j.ab.2012.04.028. Epub 2012 May 5.
In this work, we develop a methodology to quantitatively follow the solubilization of cholesterol on glycodeoxycholic acid (GDCA) micelles using (13)C nuclear magnetic resonance (NMR). The amount of solubilized cholesterol enriched in (13)C at position 4, [4-(13)C]cholesterol, was quantified from the area of its resonance, at 44.5 ppm, using the CH(2) groups from GDCA as an internal reference. The loading of the micelles with cholesterol leads to a quantitative upper field shift of most carbons in the nonpolar surface of GDCA, and this was used to follow the solubilization of unlabeled cholesterol. The solubilization followed a pseudo first-order kinetics with a characteristic time constant of 3.6 h, and the maximum solubility of cholesterol in 50 mM total lipid (GDCA + cholesterol) is 3.0 ± 0.1mM, corresponding to a mean occupation number per micelle ≥1. The solubilization profile indicates that the affinity of cholesterol for the GDCA micelles is unaffected by the presence of the solute, leading essentially to full solubilization up to the saturation limit. The relaxation times of GDCA carbons at 50mM give information regarding its aggregation and indicate that GDCA is associated in small micelles (hydrodynamic [Rh] = 1.1 nm) without any evidence for formation of larger secondary micelles. This was confirmed by dynamic light scattering results.
在这项工作中,我们开发了一种使用(13)C 核磁共振(NMR)定量跟踪胆固醇在甘氨脱氧胆酸(GDCA)胶束中溶解的方法。用 GDCA 的 CH(2)基团作为内标,通过其在 44.5ppm 处的共振峰面积,定量测定位置 4 处(13)C 标记的胆固醇([4-(13)C]胆固醇)的溶解量。胆固醇对胶束的加载导致 GDCA 非极性表面的大多数碳的定量上磁场位移,这用于跟踪未标记胆固醇的溶解。溶解遵循拟一级动力学,特征时间常数为 3.6h,50mM 总脂质(GDCA+胆固醇)中胆固醇的最大溶解度为 3.0±0.1mM,这对应于每个胶束的平均占据数≥1。溶解曲线表明,胆固醇与 GDCA 胶束的亲和力不受溶质存在的影响,基本上在达到饱和极限之前完全溶解。在 50mM 时 GDCA 碳的弛豫时间提供了关于其聚集的信息,并表明 GDCA 以小胶束(流体力学 Rh=1.1nm)存在,没有形成较大二级胶束的证据。这一点通过动态光散射结果得到了证实。