首页> 外文期刊>Journal of Lipid Research >A rapid separation technique for overcoming suppression of triacylglycerols by phosphatidylcholine using MALDI-TOF MS.
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A rapid separation technique for overcoming suppression of triacylglycerols by phosphatidylcholine using MALDI-TOF MS.

机译:一种快速分离技术,可使用MALDI-TOF MS克服磷脂酰胆碱对三酰甘油的抑制作用。

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摘要

Phospholipids and triacylglycerols (TAGs) are important classes of lipids in biological systems. Rapid methods have been developed for their characterization in crude samples, including MALDI time-of-flight MS. For mixtures, MALDI often selectively shows only some components. For example, phosphatidylcholine (PC) suppresses detection of other lipids. Most rapid MS methods detect either TAGs or phospholipids but not both. Herein, we demonstrate a simple approach to rapidly screen mixtures containing multiple lipid classes. To validate this approach, reference lipids [PC, tripalmitin (PPP), and phosphatidyl-ethanolamine (PE)] and real samples (beef, egg yolk) were used. In a binary mixture with a strong suppressor (PC), PPP was greatly suppressed. After a simple separation, suppression was virtually eliminated. A mixture of nominally nonsuppressing lipids (PE and PPP) was not adversely affected by separation. Ground beef and egg yolk were used to demonstrate detection of known lipid compositions where other methods have missed one or more lipids or lipid classes. Separation was performed using solid phase extraction with a PrepSep florisil column. A 10 min separation allows rapid screening for lipids and changes in lipids. It is sufficient to clearly detect all lipids and overcome suppression effects in complex lipid mixtures.
机译:磷脂和三酰基甘油(TAG)是生物系统中重要的脂质类别。已开发出快速方法来表征粗样品,包括MALDI飞行时间质谱仪。对于混合物,MALDI通常选择性地仅显示某些成分。例如,磷脂酰胆碱(PC)抑制其他脂质的检测。最快速的质谱方法可以检测TAG或磷脂,但不能同时检测到两者。在这里,我们演示了一种简单的方法来快速筛选包含多种脂质类别的混合物。为了验证该方法,使用了参考脂质[PC,三棕榈精蛋白(PPP)和磷脂酰乙醇胺(PE)]和实际样品(牛肉,蛋黄)。在具有强抑制剂(PC)的二元混合物中,PPP被大大抑制。简单分离后,抑制作用几乎消除了。标称非抑制性脂质(PE和PPP)的混合物不受分离的不利影响。碎牛肉和蛋黄被用来证明已知脂质成分的检测,其中其他方法未包含一种或多种脂质或脂质类别。使用固相萃取和PrepSep florisil色谱柱进行分离。 10分钟的分离可以快速筛查脂质和脂质变化。清楚地检测所有脂质并克服复杂脂质混合物中的抑制作用就足够了。

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