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首页> 外文期刊>The Biochemical Journal >A novel mass assay to quantify the bioactive lipid PtdIns3P in various biological samples.
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A novel mass assay to quantify the bioactive lipid PtdIns3P in various biological samples.

机译:一种新颖的质量检测方法,用于量化各种生物样品中的生物活性脂质PtdIns3P。

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摘要

PtdIns3P is recognized as an important player in the control of the endocytotic pathway and in autophagy. Recent data also suggest that PtdIns3P contributes to molecular mechanisms taking place at the plasma membrane and at the midbody during cytokinesis. This lipid is present in low amounts in mammalian cells and remains difficult to quantify either by traditional techniques based on radiolabelling followed by HPLC to separate the different phosphatidylinositol monophosphates, or by high-sensitive liquid chromatography coupled to MS, which is still under development. In the present study, we describe a mass assay to quantify this lipid from various biological samples using the recombinant PtdIns3P 5-kinase, PIKfyve. Using this assay, we show an increase in the mass level of PtdIns3P in mouse and human platelets following stimulation, loss of this lipid in Vps34-deficient yeasts and its relative enrichment in early endosomes isolated from BHK cells.
机译:PtdIns3P被认为是控制内吞途径和自噬的重要参与者。最新数据还表明,PtdIns3P有助于细胞质分裂过程中质膜和中体的分子机制。这种脂质在哺乳动物细胞中的含量很低,并且仍然难以通过基于放射性标记的传统技术,然后通过HPLC分离不同的磷脂酰肌醇单磷酸来进行定量,或者通过与MS偶联的高灵敏度液相色谱法(目前仍在开发中)难以定量。在本研究中,我们描述了使用重组PtdIns3P 5激酶PIKfyve从多种生物样品中定量该脂质的质量检测方法。使用该测定法,我们显示出刺激后,小鼠和人血小板中PtdIns3P的质量水平增加,Vps34缺陷型酵母中这种脂质的损失以及从BHK细胞分离的早期内体的相对富集。

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