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Human SRMAtlas: A Resource of Targeted Assays to Quantify the Complete Human Proteome

机译:Human SRMAtlas:定量完整人类蛋白质组的靶向分析资源

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摘要

The ability to reliably and reproducibly measure any protein of the human proteome in any tissue or cell type would be transformative for understanding systems-level properties as well as specific pathways in physiology and disease. Here, we describe the generation and verification of a compendium of highly specific assays that enable quantification of 99.7% of the 20,277 annotated human proteins by the widely accessible, sensitive, and robust targeted mass spectrometric method selected reaction monitoring, SRM. This human SRMAtlas provides definitive coordinates that conclusively identify the respective peptide in biological samples. We report data on 166,174 proteotypic peptides providing multiple, independent assays to quantify any human protein and numerous spliced variants, non-synonymous mutations, and post-translational modifications. The data are freely accessible as a resource at http://www.srmatlas.org/, and we demonstrate its utility by examining the network response to inhibition of cholesterol synthesis in liver cells and to docetaxel in prostate cancer lines.
机译:可靠和可重复地测量任何组织或细胞类型中人类蛋白质组中任何蛋白质的能力对于理解系统级特性以及生理和疾病的特定途径而言将具有变革性。在这里,我们描述了高度特异性的测定方法的生成和验证,该方法能够通过广泛使用,灵敏且鲁棒的靶向质谱方法选择的反应监测SRM对20,277种带注释的人类蛋白质中的99.7%进行定量。该人类SRMAtlas提供了确定的坐标,可以最终鉴定生物样品中的各个肽。我们报告了166,174个蛋白原型肽的数据,这些蛋白提供了多种独立的测定方法来定量任何人类蛋白质和许多剪接的变异体,非同义突变和翻译后修饰。该数据可从http://www.srmatlas.org/免费获得,我们通过检查对肝细胞中胆固醇合成抑制和前列腺癌系中多西紫杉醇的网络响应来证明其效用。

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