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QconCATs: design and expression of concatenated protein standards for multiplexed protein quantification

机译:QconCAT:设计和表达级联蛋白标准品以进行多重蛋白定量

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Systems biology requires knowledge of the absolute amounts of proteins in order to model biological processes and simulate the effects of changes in specific model parameters. Quantification concatamers (QconCATs) are established as a method to provide multiplexed absolute peptide standards for a set of target proteins in isotope dilution standard experiments. Two or more quantotypic peptides representing each of the target proteins are concatenated into a designer gene that is metabolically labelled with stable isotopes in Escherichia coli or other cellular or cell-free systems. Co-digestion of a known amount of QconCAT with the target proteins generates a set of labelled reference peptide standards for the unlabelled analyte counterparts, and by using an appropriate mass spectrometry platform, comparison of the intensities of the peptide ratios delivers absolute quantification of the encoded peptides and in turn the target proteins for which they are surrogates. In this review, we discuss the criteria and difficulties associated with surrogate peptide selection and provide examples in the design of QconCATs for quantification of the proteins of the nuclear factor κB pathway.
机译:系统生物学要求了解蛋白质的绝对量,以便对生物学过程进行建模并模拟特定模型参数变化的影响。建立定量辅助催化剂(QconCAT)作为在同位素稀释标准实验中为一组目标蛋白提供多重绝对肽标准品的方法。代表每种靶蛋白的两个或多个定量肽被连接到一个设计基因中,该基因在大肠杆菌或其他细胞或无细胞系统中被稳定的同位素代谢标记。将已知量的QconCAT与目标蛋白共消化可生成未标记的分析物对应物的一组标记的参考肽标准品,并通过使用适当的质谱平台,比较肽比率的强度即可对编码的肽进行绝对定量肽,然后替代它们的靶蛋白。在这篇综述中,我们讨论了与替代肽选择有关的标准和困难,并提供了设计QconCATs定量核因子κB途径蛋白的实例。

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