Churchward Matthew A, Brandman David M, Rogasevskaia Tatiana, Coorssen Jens R
Department of Physiology and Biophysics, University of Calgary Faculty of Medicine, Calgary, Alberta, Canada, T2N 4N1.
J Chem Biol. 2008 Nov;1(1-4):79-87. doi: 10.1007/s12154-008-0007-1. Epub 2008 Jun 17.
A wide range of methods exist for the on-plate detection of lipids resolved by thin layer chromatography. Fluorescence generally offers improvements in sensitivity over methods that use colorimetric or simple densitometric detection. In this paper, we report that a classic cupric sulfate charring protocol produces a fluorescent signal that sensitively and quantitatively detects a wide range of phospholipids, neutral lipids, and sterols after automated, multi-development high performance thin layer chromatography. The measured lower limits of detection and quantification, respectively, were, on average, 80 and 210 pmol for phospholipids and 43 fmol and 8.7 pmol for sterols. The simple, inexpensive, and highly sensitive approach described here was used to quantitatively analyze the lipid and sterol composition of sea urchin cortical vesicles, a stage-specific model system used to study the mechanism of regulated membrane fusion.
对于通过薄层色谱法分离的脂质进行板上检测,存在多种方法。与使用比色法或简单光密度检测的方法相比,荧光法通常在灵敏度方面具有优势。在本文中,我们报告称,一种经典的硫酸铜炭化方案会产生一种荧光信号,该信号能够在自动多次展开高效薄层色谱后灵敏且定量地检测多种磷脂、中性脂质和固醇。磷脂的检测下限和定量下限平均分别为80皮摩尔和210皮摩尔,固醇的检测下限和定量下限分别为43飞摩尔和8.7皮摩尔。本文所描述的这种简单、廉价且高度灵敏的方法被用于定量分析海胆皮质囊泡的脂质和固醇组成,海胆皮质囊泡是一种用于研究调节膜融合机制的阶段特异性模型系统。