Advances in phosphopeptide enrichment techniques for phosphoproteomics

被引:100
作者
Beltran, Luisa [1 ]
Cutillas, Pedro R. [1 ]
机构
[1] Queen Mary Univ London, John Vane Sci Ctr, Ctr Cell Signalling, Analyt Signalling Grp,Barts Canc Inst, London EC1M 6BQ, England
基金
英国医学研究理事会; 英国生物技术与生命科学研究理事会;
关键词
Mass spectrometry; Proteomics; Systems biology; Cell signaling; ION AFFINITY-CHROMATOGRAPHY; TIME-OF-FLIGHT; CALCIUM-PHOSPHATE PRECIPITATION; HIGHLY SELECTIVE ENRICHMENT; TANDEM MASS-SPECTROMETRY; PHOSPHORYLATION SITES; TITANIUM-DIOXIDE; TYROSINE PHOSPHORYLATION; PROTEIN-PHOSPHORYLATION; IN-VIVO;
D O I
10.1007/s00726-012-1288-9
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Phosphoproteomics is increasingly used to address a wide range of biological questions. However, despite some success, techniques for phosphoproteomics are not without challenges. Phosphoproteins are present in cells in low abundance relative to their unphosphorylated counterparts; therefore phosphorylated proteins (or phosphopeptides after protein digestion) are rarely detected in standard shotgun proteomics experiments. Thus, extraction of phosphorylated polypeptides from complex mixtures is a critical step in the success of phosphoproteomics experiments. Intense research over the last decade has resulted in the development of powerful techniques for phosphopeptide enrichment prior to analysis by mass spectrometry. Here, we review how the development of IMAC, MOAC, chemical derivatization and antibody affinity purification and chromatography is contributing to the evolution of phosphoproteomics techniques. Although further developments are needed for the technology to reach maturity, current state-of-the-art techniques can already be used as powerful tools for biological research.
引用
收藏
页码:1009 / 1024
页数:16
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