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Comprehensive Genome-Wide Proteomic Analysis of Human Placental Tissue for the Chromosome-Centric Human Proteome Project

机译:以染色体为中心的人胎盘组织综合基因组型蛋白质组学分析

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We believe that high-quality, extensive proteome maps are achievable within a planned 10-year period. With the well-established analytical methods, we have accomplished genome-wide proteomic analysis of placental tissue, resulting in 4,239 identified proteins that include 219 N-linked glycopeptides and 592 phosphopeptides with high confidence (FDR < 1%). Moreover, 1331 unique proteins were quantified with high confidence (FDR < 1%). In the next step, glycoproteins, phosphoproteins, and preeclampsia-specific proteins that have been identified from the initial profiling will be subjected to validation in the context of missing proteins that would fill in the predicted 20,300 gene products. With our well-established methods, protein evidence for 13 placenta-specific genes were verified. Further studies should focus on the molecular mechanism of those identified placenta-specific proteins involved in various biological systems. The analytical methods applied to this initial profiling would also contribute to the development of a standardized platform of the C-HPP. All raw data produced in the present study will be deposited in the public database and shared with all C-HPP teams.
机译:我们认为,在计划10年内,可以实现高质量,广泛的蛋白质组地图。通过良好的分析方法,我们已经完成了胎盘组织的基因组蛋白质组学分析,导致4,239个鉴定的蛋白质,包括219个连接糖肽和592种具有高置信度的磷酸肽(FDR <1%)。此外,用高置信度(FDR <1%)量化1331个独特的蛋白质。在下一步骤中,在初始分析中鉴定的糖蛋白,磷蛋白和预坦克敏的特异性蛋白质将在缺失蛋白质的上下文中进行验证,该蛋白质将填充预测的20,300个基因产物。凭借我们成熟的方法,验证了13种胎盘特异性基因的蛋白质证据。进一步的研究应专注于参与各种生物系统中鉴定的胎盘特异性蛋白质的分子机制。应用于该初始分析的分析方法也将有助于开发C-HPP的标准化平台。本研究中产生的所有原始数据将存入公共数据库并与所有C-HPP团队共享。

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