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首页> 外文期刊>Clinical Chemistry: Journal of the American Association for Clinical Chemists >Automated detection of inaccurate and imprecise transitions in peptide quantification by multiple reaction monitoring mass spectrometry.
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Automated detection of inaccurate and imprecise transitions in peptide quantification by multiple reaction monitoring mass spectrometry.

机译:通过多反应监测质谱自动检测肽定量中的不准确和不精确的过渡。

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BACKGROUND: Multiple reaction monitoring mass spectrometry (MRM-MS) of peptides with stable isotope-labeled internal standards (SISs) is increasingly being used to develop quantitative assays for proteins in complex biological matrices. These assays can be highly precise and quantitative, but the frequent occurrence of interferences requires that MRM-MS data be manually reviewed, a time-intensive process subject to human error. We developed an algorithm that identifies inaccurate transition data based on the presence of interfering signal or inconsistent recovery among replicate samples. METHODS: The algorithm objectively evaluates MRM-MS data with 2 orthogonal approaches. First, it compares the relative product ion intensities of the analyte peptide to those of the SIS peptide and uses a t-test to determine if they are significantly different. A CV is then calculated from the ratio of the analyte peak area to the SIS peak area from the sample replicates. RESULTS: The algorithm identified problematic transitions and achieved accuracies of 94%-100%, with a sensitivity and specificity of 83%-100% for correct identification of errant transitions. The algorithm was robust when challenged with multiple types of interferences and problematic transitions. CONCLUSIONS: This algorithm for automated detection of inaccurate and imprecise transitions (AuDIT) in MRM-MS data reduces the time required for manual and subjective inspection of data, improves the overall accuracy of data analysis, and is easily implemented into the standard data-analysis work flow. AuDIT currently works with results exported from MRM-MS data-processing software packages and may be implemented as an analysis tool within such software.
机译:背景:具有稳定同位素标记的内标(SIS)的多肽的多反应监测质谱(MRM-MS)越来越多地用于开发复杂生物基质中蛋白质的定量分析方法。这些测定法可以高度精确和定量,但是干扰的频繁发生要求手动检查MRM-MS数据,这是一个耗时的过程,容易出错。我们开发了一种算法,该算法根据干扰信号的存在或重复样本之间的回收率不一致来识别不准确的过渡数据。方法:该算法通过2种正交方法客观地评估MRM-MS数据。首先,它将分析物肽的相对产物离子强度与SIS肽的相对产物离子强度进行比较,并使用t检验确定它们是否显着不同。然后从样品重复样品中分析物峰面积与SIS峰面积之比计算出CV。结果:该算法识别出有问题的过渡,并获得了94%-100%的准确度,对于正确识别错误的过渡,其灵敏度和特异性为83%-100%。当遇到多种类型的干扰和有问题的过渡时,该算法是可靠的。结论:该算法可自动检测MRM-MS数据中的不准确和不精确转换(AuDIT),从而减少了手动和主观检查数据所需的时间,提高了数据分析的整体准确性,并且易于在标准数据分析中实施工作流程。 AuDIT当前可以处理从MRM-MS数据处理软件包中导出的结果,并且可以作为此类软件中的分析工具来实现。

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