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Biases in the Experimental Annotations of Protein Function and Their Effect on Our Understanding of Protein Function Space

机译:蛋白质功能实验注释中的偏见及其对我们对蛋白质功能空间的理解的影响

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The ongoing functional annotation of proteins relies upon the work of curators to capture experimental findings from scientific literature and apply them to protein sequence and structure data. However, with the increasing use of high-throughput experimental assays, a small number of experimental studies dominate the functional protein annotations collected in databases. Here, we investigate just how prevalent is the “few articles - many proteins” phenomenon. We examine the experimentally validated annotation of proteins provided by several groups in the GO Consortium, and show that the distribution of proteins per published study is exponential, with 0.14% of articles providing the source of annotations for 25% of the proteins in the UniProt-GOA compilation. Since each of the dominant articles describes the use of an assay that can find only one function or a small group of functions, this leads to substantial biases in what we know about the function of many proteins. Mass-spectrometry, microscopy and RNAi experiments dominate high throughput experiments. Consequently, the functional information derived from these experiments is mostly of the subcellular location of proteins, and of the participation of proteins in embryonic developmental pathways. For some organisms, the information provided by different studies overlap by a large amount. We also show that the information provided by high throughput experiments is less specific than those provided by low throughput experiments. Given the experimental techniques available, certain biases in protein function annotation due to high-throughput experiments are unavoidable. Knowing that these biases exist and understanding their characteristics and extent is important for database curators, developers of function annotation programs, and anyone who uses protein function annotation data to plan experiments.
机译:蛋白质的持续功能注释依赖于策委的工作,以捕获来自科学文献的实验结果,并将它们应用于蛋白质序列和结构数据。然而,随着高通量实验测定的越来越多,少量的实验研究主要占据数据库中收集的功能蛋白质注释。在这里,我们只调查普遍是“少数文章 - 许多蛋白质”现象。我们研究了在GO联盟中的几个组提供的实验验证的蛋白质注释,并表明每种公开研究的蛋白质分布是指数级的,其中0.14%的物品提供了在UNIPROT中为25%的蛋白质的注释来源 - 果阿汇编。由于每个主导物品描述了使用可以发现一个功能或一小组功能的测定,因此这导致我们对许多蛋白质的功能所了解的大量偏见。质谱,显微镜和RNAI实验支配高通量实验。因此,源自这些实验的功能信息主要是蛋白质的亚细胞位置,以及蛋白质在胚胎发育途径中的参与。对于某些生物,不同研究提供的信息重叠大量。我们还表明,通过低通量实验提供的高通量实验提供的信息较低。鉴于可用的实验技术,由于高通量实验引起的蛋白质函数注释中的某些偏差是不可避免的。知道这些偏差存在并理解其特征和程度对于数据库策展人,功能注释程序的开发人员以及使用蛋白质功能注释数据来规划实验的人来说很重要。

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