Protocol for micro-purification, enrichment, pre-fractionation and storage of peptides for proteomics using StageTips

被引:3014
作者
Rappsilber, Juri [1 ]
Mann, Matthias [2 ]
Ishihama, Yasushi [3 ,4 ]
机构
[1] Univ Edinburgh, Wellcome Trust Ctr Cell Biol, Edinburgh, Midlothian, Scotland
[2] Max Planck Inst Biochem, D-82152 Martinsried, Germany
[3] Keio Univ, Inst Adv Biosci, Yamagata, Japan
[4] Japan Sci & Technol Agcy, PRESTO, Tokyo, Japan
关键词
D O I
10.1038/nprot.2007.261
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Mass spectrometry (MS)-based proteomics measures peptides derived from proteins by proteolytic cleavage. Before performing the analysis by matrix-assisted laser desorption/ionization-tandem mass spectrometry (MALDI-MS/MS), nanoelectrospray-MS/MS (NanoES-MS/MS) or liquid chromatography-MS/MS (LC-MS/MS), the peptide mixtures need to be cleaned, concentrated and often selectively enriched or pre-fractionated, for which we employ simple, self-made and extremely economical stop-and-go-extraction tips (StageTips). StageTips are ordinary pipette tips containing very small disks made of beads with reversed phase, cation-exchange or anion-exchange surfaces embedded in a Teflon mesh. The fixed nature of the beads allows flexible combination of disks with different surfaces to obtain multi-functional tips. Disks containing different surface functionalities and loose beads such as titania and zirconia for phosphopeptide enrichment can be combined. Incorporation into an automated workflow has also been demonstrated. Desalting and concentration takes approximately 5 min while fractionation or enrichment takes approximately 30 min.
引用
收藏
页码:1896 / 1906
页数:11
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