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首页> 外文期刊>Journal of proteome research >Determination and comparison of the Francisella tularensis subsp. novicida U112 proteome to other bacterial proteomes
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Determination and comparison of the Francisella tularensis subsp. novicida U112 proteome to other bacterial proteomes

机译:图拉弗朗西斯菌的亚种的测定和比较。 Novicida U112蛋白质组到其他细菌蛋白质组

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摘要

The proteins expressed by Francisella tularensis subsp. novicida U112 grown to midexponential phase were surveyed by nanoLC-tandem mass spectrometry (LC-MS/MS). To improve annotation of the genome and develop a technology to provide high-throughput analysis of the Francisella proteome in multiple conditions, we sought to establish a fast and simple analysis that would reduce as much as possible the false discovery rate. Our survey detected expression of 63.0% of the predicted proteome from the stable condition of growth in rich medium available at (www.francisella.org). On the basis of detection of essential proteins, we estimated coverage to be approximately 80% of the actual expressed proteome. This suggests that no less than 70% of the proteins could be expressed in this condition. This analysis revealed two previously unidentified protein coding open reading frames and validated 50% of the proteins annotated as hypothetical. On the basis of results of the screen to detect essential proteins, not all proteins expressed provide a measurable contribution to F.t. novicida growth in this condition. Comparison of this protein profile with other profiles previously published suggested that the genome size and number of genes involved in regulation have little effect on the number of proteins expressed in a given stable condition.
机译:图拉弗朗西斯菌亚种表达的蛋白质。通过nanoLC-串联质谱法(LC-MS / MS)调查了生长到中指数期的Novicida U112。为了改善基因组的注释并开发一种技术以在多种情况下提供弗朗西斯菌蛋白质组的高通量分析,我们试图建立一种快速简单的分析方法,以尽可能减少错误发现率。我们的调查从(www.francisella.org)提供的丰富培养基的稳定生长条件中检测到63.0%的预测蛋白质组表达。在检测必需蛋白质的基础上,我们估计覆盖率约为实际表达的蛋白质组的80%。这表明在这种条件下可以表达不少于70%的蛋白质。该分析揭示了两个先前未鉴定的编码开放阅读框的蛋白质,并验证了50%的假设蛋白质。根据检测必需蛋白质的筛选结果,并非所有表达的蛋白质都能为F.t.诺维达在这种情况下生长。将该蛋白质图谱与先前发表的其他图谱进行比较表明,基因组大小和参与调控的基因数对在给定的稳定条件下表达的蛋白质数影响很小。

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