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首页> 外文期刊>The Biochemical Journal >Subcellular localization of phosphatidylinositol 4,5-bisphosphate using the pleckstrin homology domain of phospholipase C delta(1)
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Subcellular localization of phosphatidylinositol 4,5-bisphosphate using the pleckstrin homology domain of phospholipase C delta(1)

机译:使用磷脂酶C delta的pleckstrin同源域在磷脂酰肌醇4,5-二磷酸中进行亚细胞定位(1)

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摘要

Ptd(4.5)P-2 is thought to promote and organize a wide range of cellular functions, including vesicular membrane traffic and cytoskeletal dynamics. by recruiting functional protein complexes to restricted locations in cellular membranes. However, little is known about the distribution of PtdIns(4,5)P-2 in the cell at high resolution. We have used the pleckstrin homology (PH) domain of phospholipase delta(1) (PLCdelta(1)), narrowly specific for PtdIns(4,5)P-2. to map the distribution of the lipid in astrocytoma and A431 cells. We applied the glutathione S-transferase-tagged PLCdelta(1) PH domain (PLCdelta(1)PH-GST) in an on-section labelling approach which avoids transfection procedures. Here we demonstrate PtdIns(4,5)P-2 labelling in the plasma membrane, and also in intracellular membranes, including Golgi (mainly stack), endosomes and endoplasmic reticulum, as well as in electron-dense structures within the nucleus. At the plasma membrane, labelling was more concentrated over lamellipodia, but not in caveolae, which contained less than 10% of the total cell-surface labelling. A dramatic decrease in signal over labelled compartments was observed on preincubation with the cognate headgroup [Ins(1,4,5)P-3], and plasma-membrane labelling was substantially decreased after stimulation with thrombin-receptor-activating peptide (SFLLRN in the one-letter amino acid code), a treatment which markedly diminishes PtdIns(4.5)P-2 levels. Thus we have developed a highly selective method for mapping the PtdIns(4,5)P-2 distribution within cells at high resolution. and our data provide direct evidence for this lipid at key functional locations.
机译:Ptd(4.5)P-2被认为可以促进和组织广泛的细胞功能,包括水泡膜运输和细胞骨架动力学。通过将功能性蛋白质复合物募集到细胞膜的受限位置。但是,关于PtdIns(4,5)P-2在细胞中的高分辨率分布了解甚少。我们已使用磷脂酶delta(1)(PLCdelta(1))的pleckstrin同源性(PH)域,对PtdIns(4,5)P-2具有狭义特异性。绘制脂质在星形细胞瘤和A431细胞中的分布图。我们应用了谷胱甘肽S-转移酶标记的PLCdelta(1)PH域(PLCdelta(1)PH-GST)的局部标记方法,避免了转染程序。在这里,我们展示了质膜以及细胞内膜(包括高尔基体(主要是堆叠),内体和内质网)以及细胞核内电子致密结构中的PtdIns(4,5)P-2标记。在质膜上,标记更多地集中在片状脂膜上,而不是在海绵状膜中,而在海绵状膜中,细胞膜的标记少于全部细胞表面标记的10%。在与同源头基团[Ins(1,4,5)P-3]一起预孵育时,观察到信号在标记的区室中急剧减少,并且在凝血酶受体激活肽(SFLLRN in (一个字母的氨基酸代码),该处理可显着降低PtdIns(4.5)P-2的水平。因此,我们已经开发出了一种高度选择性的方法,用于以高分辨率映射细胞内的PtdIns(4,5)P-2分布。我们的数据为这种脂质在关键功能部位提供了直接的证据。

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