Characterization and quantitation of membrane proteomes using multidimensional MS-based proteomic technologies

被引:29
作者
Blonder, J [1 ]
Conrads, TP [1 ]
Veenstra, TD [1 ]
机构
[1] NCI, SAIC Frederick Inc, Lab Proteom & Analyt Technol, Frederick, MD 21702 USA
关键词
isotopic labeling; mass spectrometry; membrane proteomics; multidimensional fractionation; quantitation;
D O I
10.1586/14789450.1.2.153
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A major goal of proteomics is to develop methods that enable the systematic characterization of every protein within the cell or particular subcellular proteome using a single analytical platform. Although the equivalent has already been achieved in genomics, reaching this goal in proteomics represents a much greater challenge due to the wide dynamic range of protein expression, numerous post-translational modifications and remarkable physicochemical heterogeneity of proteins. A major analytical challenge has Involved developing more effective means for proteome-scale investigations of membrane proteins, whose solubility differs drastically from that of cytoplasmic proteins. Fortunately, rapid progress has Increased the ability to characterize this critically important class of proteins on a scale analogous to that of aqueous soluble proteins.
引用
收藏
页码:153 / 163
页数:11
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