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首页> 外文期刊>Journal of Molecular Biology >Life's simple measures: Unlocking the proteome
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Life's simple measures: Unlocking the proteome

机译:生活中的简单措施:释放蛋白质组

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摘要

Using modified nucleotides and selecting for slow off-rates in the SELEX procedure, we have evolved a special class of aptamers, called SOMAmers (slow off-rate modified aptamers), which bind tightly and specifically to proteins in body fluids. We use these in a novel assay that yields 1:1 complexes of the SOMAmers with their cognate proteins in body fluids. Measuring the SOMAmer concentrations of the resultant complexes reflects the concentration of the proteins in the fluids. This is simply done by hybridization to complementary sequences on solid supports, but it can also be done by any other DNA quantification technology (including NexGen sequencing). We use measurements of over 1000 proteins in under 100 μL of serum or plasma to answer important medical questions, two of which are reviewed here. A number of bioinformatics methods have guided our discoveries, including principal component analysis. We use various methods to evaluate sample handling procedures in our clinical samples and can identify many parameters that corrupt proteomics analysis.
机译:通过使用修饰的核苷酸并在SELEX程序中选择慢解离速率,我们已经进化出一类特殊的适体,称为SOMAmers(慢解离速率修饰的适体),它与体液中的蛋白质紧密结合,并且特异性结合。我们将它们用于一种新颖的检测方法,该检测方法可在体液中产生SOMAmers及其同源蛋白的1:1复合物。测量所得复合物的SOMAmer浓度反映了液体中蛋白质的浓度。简单地通过与固相支持物上的互补序列杂交即可完成,但也可以通过任何其他DNA定量技术(包括NexGen测序)来完成。我们使用100μL以下血清或血浆中1000多种蛋白质的测量值来回答重要的医学问题,此处对其中两个进行了综述。许多生物信息学方法指导了我们的发现,包括主成分分析。我们使用各种方法来评估临床样品中的样品处理程序,并可以识别出破坏蛋白质组学分析的许多参数。

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