Peptide fractionation in proteomics approaches

被引:35
作者
Manadas, Bruno [1 ,2 ]
Mendes, Vera M. [1 ]
English, Jane [2 ]
Dunn, Michael J. [2 ]
机构
[1] Univ Coimbra, Prote Unit, Ctr Neurosci & Cell Biol, Nucleo 04, P-3060197 Cantanhede, Portugal
[2] Univ Coll Dublin, UCD Conway Inst, Sch Med & Med Sci, Dublin 2, Ireland
基金
爱尔兰科学基金会;
关键词
mass spectrometry; multidimensional liquid chromatography; peptide fractionation; proteomics; PERFORMANCE LIQUID-CHROMATOGRAPHY; STRONG-CATION-EXCHANGE; REVERSED-PHASE; PROTEIN IDENTIFICATION; SHOTGUN PROTEOMICS; MASS-SPECTROMETRY; PROTEOTYPIC PEPTIDES; PH GRADIENT; SEPARATION; OFFGEL;
D O I
10.1586/EPR.10.46
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Peptide fractionation is extremely important in proteomics approaches. Full proteome characterization is desired from complex organisms, and with growing interest in post-translational modifications an extended protein sequence coverage is required. Peptide fractionation techniques have the great challenge of feeding current mass spectrometers in a way in which these issues are met. Peptide fractionation can be divided into three simple components: the column characteristics; the mobile phase; and peptide properties (charge, polarity, hydrophobicity and size). The current challenges are in the combination of these three components to allow comprehensive proteomics studies to be improved.
引用
收藏
页码:655 / 663
页数:9
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