期刊
ANALYTICA CHIMICA ACTA
卷 909, 期 -, 页码 67-74出版社
ELSEVIER SCIENCE BV
DOI: 10.1016/j.aca.2016.01.008
关键词
Sample preparation; Phosphoproteomics; Polydopamine; Ti4+-immobilized metal-ion affinity chromatography; Shotgun proteomics; Magnetic solid phase extraction
资金
- Sapienza Universita di Roma [C26A15WBLF]
Protein post translational modifications currently represent one of the main challenges with proteomic analysis, due to the important biological role they play within cells. Protein phosphorylation is one of the most important, with several approaches developed for phosphopeptides enrichment and analysis, essential for comprehensive phosphoproteomic analysis. However, the development of new materials for phosphopeptides enrichment may overcome previous drawbacks and improve enrichment of such peptides. In this regard, new magnetic stationary phases based on polydopamine coating and Ti4+ immobilization exploit the potential of IMAC enrichment and couple it with the versatility of magnetic solid phase extraction. In this work the use of such stationary phase was extended from the MALDI proof of concept stage with the development of an optimized method for phosphopeptides enrichment compatible with typical shotgun proteomics experimental workflows. Different loading and elution buffers were tested to improve phosphopeptides recovery and enrichment selectivity. Finally, the analysis of isolated peptides pointed out that polydopamine alone is an ideal support matrix for polar post translational modifications because it enables to reduce unspecific binding and preferentially binds hydrophilic peptides. (C) 2016 Elsevier B.V. All rights reserved.
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