Phosphoinositide profiling in complex lipid mixtures using electrospray ionization mass spectrometry

被引:201
作者
Wenk, MR
Lucast, L
Di Paolo, G
Romanelli, AJ
Suchy, SF
Nussbaum, RL
Cline, GW
Shulman, GI
McMurray, W
De Camilli, P
机构
[1] Yale Univ, Sch Med, Boyer Ctr Mol Med, Howard Hughes Med Inst,Dept Cell Biol, New Haven, CT 06511 USA
[2] Yale Univ, Sch Med, Dept Internal Med, Howard Hughes Med Inst, New Haven, CT 06511 USA
[3] Yale Univ, Sch Med, Boyer Ctr Mol Med, WM Keck Mass Spectrometry Resource, New Haven, CT 06511 USA
[4] NHGRI, NIH, Bethesda, MD 20892 USA
关键词
D O I
10.1038/nbt837
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Phosphoinositides (phosphorylated derivatives of phosphatidylinositol, PI) are versatile intracellular signaling lipids whose occurrence in low concentrations complicates direct mass measurements(1-3). Here we present a sensitive method to detect, identify and quantify phosphatidylinositol phosphate (PIP) and phosphatidylinositol bisphosphate (PIP 2) with different fatty acid compositions (phosphoinositide profiles) in total lipid extracts by electrospray ionization mass spectrometry (ESI-MS). Using this method, we detected elevated concentrations of PIP2 in human fibroblasts from patients with Lowe syndrome, a genetic disorder that affects lphosphoinositide metabolism(4). Saccharomyces cerevisiae cells deficient in enzymes involved in PIP metabolism-Sac1p, a phosphoinositide phosphatase(5), and Vps34p and Pik1p, a PI 3-kinase(6) and PI 4-kinase(7), respectively-showed not only different PIP concentrations but also differential changes in PIP profiles indicating metabolic and/or subcellular pooling. Mass spectrometric analysis of phosphoinositides offers unique advantages over existing approaches and may represent a powerful diagnostic tool for human diseases that involve defective phosphoinositide metabolism.
引用
收藏
页码:813 / 817
页数:5
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