A sensitive mass spectrometric method for hypothesis-driven detection of peptide post-translational modifications: multiple reaction monitoring-initiated detection and sequencing (MIDAS)

被引:73
作者
Unwin, Richard D. [1 ]
Griffiths, John R. [1 ]
Whetton, Anthony D. [1 ]
机构
[1] Univ Manchester, Fac Med & Human Sci, Stem Cell & Leukaemia Prote Lab, Manchester, Lancs, England
基金
英国生物技术与生命科学研究理事会;
关键词
PHOSPHORYLATION SITES; PROTEIN-PHOSPHORYLATION; IDENTIFICATION; DIGESTION; STRATEGY; KINASES; TARGET;
D O I
10.1038/nprot.2009.57
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The application of a targeted mass spectrometric workflow to the sensitive identification of post-translational modifications is described. This protocol employs multiple reaction monitoring (MRM) to search for all putative peptides specifically modified in a target protein. Positive MRMs trigger an MS/MS experiment to confirm the nature and site of the modification. This approach, termed MIDAS (MRM-initiated detection and sequencing), is more sensitive than approaches using neutral loss scanning or precursor ion scanning methodologies, due to a more efficient use of duty cycle along with a decreased background signal associated with MRM. We describe the use of MIDAS for the identification of phosphorylation, with a typical experiment taking just a couple of hours from obtaining a peptide sample. With minor modifications, the MIDAS method can be applied to other protein modifications or unmodified peptides can be used as a MIDAS target.
引用
收藏
页码:870 / 877
页数:8
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