首页> 外文期刊>Rapid Communications in Mass Spectrometry: RCM >Protein abundance quantification in embryonic stem cells using incomplete metabolic labelling with N-15 amino acids, matrix-assisted laser desorption/ionisation time-of-flight mass spectrometry, and analysis of relative isotopologue abundances of pep
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Protein abundance quantification in embryonic stem cells using incomplete metabolic labelling with N-15 amino acids, matrix-assisted laser desorption/ionisation time-of-flight mass spectrometry, and analysis of relative isotopologue abundances of pep

机译:使用N-15氨基酸的不完全代谢标记,基质辅助激光解吸/电离飞行时间质谱法和pep的相对同位素体丰度分析,对胚胎干细胞中的蛋白质丰度进行定量

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摘要

An isotope dilution method for protein quantification is presented in the context of matrix-assisted laser desorption/ionisation time-of-flight mass spectrometry (MALDI-TOFMS) and mass fingerprinting experiments, revealing an unappreciated high reproducibility and accuracy of relative peak intensity measurements. Labelled proteins were generated by growing cells in a medium containing N-15-enriched amino acids, and were mixed with proteins of natural isotopic composition from control cells in ratios of approximately 0:1, 1:7,1:2, 2:1, 7:1, and 1:0 (labelled/unlabelled). Mixtures were separated by two-dimensional gel electrophoresis and analysed by MALDI-TOFMS using typical experimental conditions. A linear relationship is demonstrated between the relative isotopologue abundances (RLA values) for particular peaks in the isotopic distribution of tryptic peptide fragments of the proteins, and the mole fractions of labelled proteins in the mixture. Analysis of RLA values (ARIA quantification) for peptides of six typical silver-stained protein spots for the various mixtures could reproduce the experimentally contrived ratios with approximate errors between 4% (2:1 mixture) and about 18% (1:7 mixture). A consideration of error and its propagation is discussed. ARIA does not require complete separation of the isotope patterns of labelled and unlabelled peptides, and is therefore advantageous in combination with all kinds of labelling experiments in biological systems, because it is compatible with minimal metabolic incorporation of labelling reagent. Simulations indicate that the minimum required N-15 enrichment of the total amino acid pool sufficient for ARIA is less than 4%. In an accompanying paper in this issue, we apply ARIA to proteins differentially labelled with isotope-coded alkylation reagents. Copyright (C) 2003 John Wiley Sons, Ltd. [References: 37]
机译:在基质辅助激光解吸/电离飞行时间质谱(MALDI-TOFMS)和质谱指纹图谱实验的背景下,提出了一种用于蛋白质定量的同位素稀释法,揭示了相对峰值强度测量的高再现性和准确性。标记的蛋白质是通过使细胞在含有N-15富集的氨基酸的培养基中生长而生成的,并与来自对照细胞的天然同位素组成的蛋白质以大约0:1、1:7、1:2、2:1的比例混合,7:1和1:0(标记/未标记)。通过二维凝胶电泳分离混合物,并使用典型的实验条件通过MALDI-TOFMS进行分析。在蛋白质的胰蛋白酶消化的肽片段的同位素分布中,特定峰的相对同位素体丰度(RLA值)与混合物中标记蛋白质的摩尔分数之间存在线性关系。分析各种混合物中六个典型的银染蛋白斑点的肽段的RLA值(ARIA定量),可以重现实验设计的比率,近似误差在4%(2:1混合物)和大约18%(1:7混合物)之间。讨论了错误及其传播的考虑。 ARIA不需要完全分离标记和未标记肽的同位素模式,因此与生物系统中的各种标记实验结合使用时具有优势,因为它与标记试剂的新陈代谢最少兼容。模拟表明,足以用于ARIA的总氨基酸库中的N-15富集的最低要求小于4%。在本期的随附论文中,我们将ARIA应用于经同位素编码的烷基化试剂差异标记的蛋白质。版权所有(C)2003 John Wiley Sons,Ltd. [参考:37]

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