Relative protein quantitation with post translational modifications in mass spectrometry based proteomics

J. Allmer
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Abstract

Mass spectrometry has become the tool of choice for most investigations in proteomics. Identification of proteins from complex mixtures has long been achieved and is now routinely used in countless high throughput studies. Quantitation by mass spectrometry is comparably newer and many different strategies have been proposed. One such strategy quantitates the difference in protein expression level among samples via extracted ion chromatograms, or spectral counts or a combination thereof. Another strategy involves mass modifications of the analytes in one or more of the samples under investigation. MSMAG has been developed as an extension to 2DB and it has been shown that it can aid in quantitation of data from experiments employing label-free quantitation. Recently, it has been extended to allow for analysis of data based on labelling strategies. This also makes it possible to quickly visualize and investigate inherent mass differences as presented by post translational modifications.
基于质谱的蛋白质组学中翻译后修饰的相对蛋白质定量
质谱法已成为大多数蛋白质组学研究的首选工具。从复杂混合物中鉴定蛋白质已经很长时间了,现在已经常规地用于无数的高通量研究。质谱定量相对较新,提出了许多不同的策略。一种这样的策略通过提取的离子色谱图或光谱计数或其组合来定量样品之间蛋白质表达水平的差异。另一种策略涉及对一个或多个被调查样品中的分析物进行大量修饰。MSMAG已发展为2DB的扩展,并已证明它可以帮助采用无标记定量的实验数据的定量。最近,它已扩展到允许对基于标签策略的数据进行分析。这也使得快速可视化和调查翻译后修饰所呈现的固有质量差异成为可能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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