Prasain Jeevan K, Hoang Hieu D, Edmonds Johnathan W, Miller Michael A
Department of Pharmacology and Toxicology, University of Alabama at Birmingham, AL, USA.
J Vis Exp. 2013 Jun 25(76):50447. doi: 10.3791/50447.
Caenorhabditis elegans is emerging as a powerful animal model to study the biology of lipids(1-9). Prostaglandins are an important class of eicosanoids, which are lipid signals derived from polyunsaturated fatty acids (PUFAs)(10-14). These signalling molecules are difficult to study because of their low abundance and reactive nature. The characteristic feature of prostaglandins is a cyclopentane ring structure located within the fatty acid backbone. In mammals, prostaglandins can be formed through cyclooxygenase enzyme-dependent and -independent pathways(10,15). C. elegans synthesizes a wide array of prostaglandins independent of cyclooxygenases(6,16,17). A large class of F-series prostaglandins has been identified, but the study of eicosanoids is at an early stage with ample room for new discoveries. Here we describe a procedure for extracting and analyzing prostaglandins and other eicosanoids. Charged lipids are extracted from mass worm cultures using a liquid-liquid extraction technique and analyzed by liquid chromatography coupled to electrospray ionization tandem mass spectrometry (LC-ESI-MS/MS). The inclusion of deuterated analogs of prostaglandins, such as PGF2 α-d4 as an internal standard is recommended for quantitative analysis. Multiple reaction monitoring or MRM can be used to quantify and compare specific prostaglandin types between wild-type and mutant animals. Collision-induced decomposition or MS/MS can be used to obtain information on important structural features. Liquid chromatography mass spectrometry (LC-MS) survey scans of a selected mass range, such as m/z 315-360 can be used to evaluate global changes in prostaglandin levels. We provide examples of all three analyses. These methods will provide researchers with a toolset for discovering novel eicosanoids and delineating their metabolic pathways.
秀丽隐杆线虫正逐渐成为研究脂质生物学的强大动物模型(1-9)。前列腺素是一类重要的类花生酸,它们是源自多不饱和脂肪酸(PUFA)的脂质信号(10-14)。由于这些信号分子丰度低且具有反应性,因此很难进行研究。前列腺素的特征是位于脂肪酸主链内的环戊烷环结构。在哺乳动物中,前列腺素可通过环氧化酶依赖性和非依赖性途径形成(10,15)。秀丽隐杆线虫可独立于环氧化酶合成多种前列腺素(6,16,17)。已鉴定出一大类F系列前列腺素,但类花生酸的研究尚处于早期阶段,有很大的新发现空间。在这里,我们描述了一种提取和分析前列腺素及其他类花生酸的方法。使用液-液萃取技术从大量虫体培养物中提取带电脂质,并通过液相色谱与电喷雾电离串联质谱(LC-ESI-MS/MS)进行分析。建议加入前列腺素的氘代类似物,如PGF2α-d4作为内标进行定量分析。多反应监测或MRM可用于定量和比较野生型和突变动物之间特定前列腺素类型。碰撞诱导分解或MS/MS可用于获取重要结构特征的信息。选定质量范围(如m/z 315-360)的液相色谱质谱(LC-MS)扫描可用于评估前列腺素水平的整体变化。我们提供了所有三种分析的示例。这些方法将为研究人员提供一套工具,用于发现新型类花生酸并描绘其代谢途径。