Sandhoff R, Brügger B, Jeckel D, Lehmann W D, Wieland F T
Biochemie-Zentrum Heidelberg (BZH), University of Heidelberg, Im Neuenheimer Feld 328, 69120 Heidelberg, Germany.
J Lipid Res. 1999 Jan;40(1):126-32.
A mass spectrometric method for the quantification of free cholesterol in cells and subcellular membranes is presented. The method is based on a simple one-step chemical derivatization of cholesterol to cholesterol-3-sulfate by a sulfur trioxide-pyridine complex. Quantification is performed by nano-electrospray ionization tandem mass spectrometry (nanoESI-MS/MS) using a stable isotope labeled internal standard. The determination of free cholesterol is demonstrated in about 250 cells of a Chinese hamster ovary (CHO) cell line. With this method a molar ratio of free cholesterol to total phospholipids of 0.34 mol/mol in CHO cells was determined. In a subcellular membrane fraction enriched in Golgi membranes, a molar ratio of free cholesterol to total phospholipids of 0.57 mol/mol was determined. The method should be of value for quantification of other sterols as demonstrated for ergosterol and stigmasterol.
本文介绍了一种用于定量细胞和亚细胞膜中游离胆固醇的质谱方法。该方法基于通过三氧化硫 - 吡啶络合物将胆固醇简单一步化学衍生为胆固醇 - 3 - 硫酸盐。使用稳定同位素标记的内标通过纳米电喷雾电离串联质谱法(nanoESI-MS/MS)进行定量。在中国仓鼠卵巢(CHO)细胞系的约250个细胞中证明了游离胆固醇的测定。用该方法测定CHO细胞中游离胆固醇与总磷脂的摩尔比为0.34 mol/mol。在富含高尔基体膜的亚细胞膜组分中,测定游离胆固醇与总磷脂的摩尔比为0.57 mol/mol。如对麦角固醇和豆甾醇所示,该方法对于其他甾醇的定量应该是有价值的。