Advances in Quantitative Mass Spectrometry Analysis: Weighing in on Isotope Coding and Label-Free Approaches for Expression and Functional Proteomics

被引:2
|
作者
Chien, Ko-yi [1 ]
Goshe, Michael B. [1 ]
机构
[1] N Carolina State Univ, Dept Mol & Struct Biochem, Raleigh, NC 27695 USA
基金
美国农业部;
关键词
Mass spectrometry; Quantitative proteomics; Phosphoproteomics; Isotope coding; Label-free quantitation; Absolute quantitation; ELECTRON-CAPTURE DISSOCIATION; CODED AFFINITY TAGS; COMPLEX PROTEIN MIXTURES; MULTIDIMENSIONAL LIQUID-CHROMATOGRAPHY; PEPTIDYL-LYS METALLOENDOPEPTIDASE; CATALYZED O-16-TO-O-18 EXCHANGE; DIFFERENCE GEL-ELECTROPHORESIS; N-LINKED GLYCOPROTEINS; ACCURATE MASS; CANCER-CELLS;
D O I
10.2174/157341109787846126
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Mass spectrometry is an extremely versatile analytical technique that is capable of characterizing proteins at various levels of biochemical sophistication from recognition of protein components and their modifications to their quantification within a sample. With the development of electrospray ionization and matrix-assisted laser desorption ionization, the last decade of protein analysis using mass spectrometry has fully established the field of proteomics within the life sciences and a major player in the systems biology paradigm. The diversity of proteins and their multi-facetted functions are indicative of the numerous mass spectrometry methods that are used in quantitative proteomic analysis. In this review, the various techniques developed to quantify protein abundance by mass spectrometry are presented in terms of those associated with both stable isotope coding and label-free strategies. The implementation of these methods to the quantitative mass spectrometry analysis from "proof-of-concept" to those that tackle investigations of protein expression and those of protein function mediated by post-translation modifications are also discussed.
引用
收藏
页码:166 / 185
页数:20
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