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Quantitative maps of protein phosphorylation sitesacross 14 different rat organs and tissues

机译:跨越14种不同大鼠器官和组织的蛋白质磷酸化位点的定量图

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摘要

Deregulated cellular signalling is a common hallmark of disease, and delineating tissuephosphoproteomes is key to unravelling the underlying mechanisms. Here we present thebroadest tissue catalogue of phosphoproteins to date, covering 31,480 phosphorylation siteson 7,280 proteins quantified across 14 rat organs and tissues. We provide the data set as aneasily accessible resource via a web-based database, the CPR PTm Resource. A major fractionof the presented phosphorylation sites are tissue-specific and modulate protein interactionnetworks that are essential for the function of individual organs. For skeletal muscle, we findthat phosphotyrosines are over-represented, which is mainly due to proteins involved inglycogenolysis and muscle contraction, a finding we validate in human skeletal muscle biopsies.Tyrosine phosphorylation is involved in both skeletal and cardiac muscle contraction, whereasglycogenolytic enzymes are tyrosine phosphorylated in skeletal muscle but not in the liver. Thepresented phosphoproteomic method is simple and rapid, making it applicable for screening ofdiseased tissue samples.
机译:失调的细胞信号传导是疾病的常见标志,而组织磷酸化蛋白质组的描绘是揭示潜在机制的关键。在这里,我们介绍了迄今为止最广泛的磷蛋白组织目录,涵盖了在14个大鼠器官和组织中定量的7,480个蛋白中的31,480个磷酸化位点。我们通过基于Web的数据库CPR PTm资源将数据集作为易于访问的资源提供。所呈现的磷酸化位点的主要部分是组织特异性的,并且调节蛋白质相互作用网络,这对于单个器官的功能至关重要。对于骨骼肌,我们发现磷酸酪氨酸含量过高,这主要归因于参与糖原分解和肌肉收缩的蛋白质,我们在人体骨骼肌活检中证实了这一发现。酪氨酸磷酸化参与骨骼肌和心肌的收缩,而糖原分解酶是酪氨酸。在骨骼肌中磷酸化,但在肝脏中不磷酸化。提出的磷酸化蛋白质组学方法简便,快速,可用于筛查病变组织样品。

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