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Fractionation of Enriched Phosphopeptides Using pH/Acetonitrile-Gradient-Reversed-Phase Microcolumn Separation in Combination with LC-MS/MS Analysis
M. Ondrej, P. Rehulka, H. Rehulkova, R. Kupcik, A. Tichy
Jazyk angličtina Země Švýcarsko
Typ dokumentu časopisecké články
Grantová podpora
long-term organization development plan Medical Aspects of Weapons of Mass Destruction of the Faculty of Military Health Sciences
Ministry of Defense of the Czech Republic
NV19-02-00297
Ministry of Health of the Czech Republic
NLK
Free Medical Journals
od 2000
Freely Accessible Science Journals
od 2000
PubMed Central
od 2007
Europe PubMed Central
od 2007
ProQuest Central
od 2000-03-01
Open Access Digital Library
od 2000-01-01
Open Access Digital Library
od 2007-01-01
Health & Medicine (ProQuest)
od 2000-03-01
ROAD: Directory of Open Access Scholarly Resources
od 2000
PubMed
32492839
DOI
10.3390/ijms21113971
Knihovny.cz E-zdroje
- MeSH
- acetonitrily chemie MeSH
- chemická frakcionace metody MeSH
- chromatografie kapalinová metody MeSH
- fosfopeptidy chemie MeSH
- fosfoproteiny metabolismus MeSH
- koncentrace vodíkových iontů MeSH
- lidé MeSH
- nádorové buněčné linie MeSH
- proteom MeSH
- proteomika MeSH
- tandemová hmotnostní spektrometrie metody MeSH
- titan chemie MeSH
- tlak MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
Mass spectrometry (MS) is a powerful and sensitive method often used for the identification of phosphoproteins. However, in phosphoproteomics, there is an identified need to compensate for the low abundance, insufficient ionization, and suppression effects of non-phosphorylated peptides. These may hamper the subsequent liquid chromatography-mass spectrometry/mass spectrometry (LC-MS/MS) analysis, resulting in incomplete phosphoproteome characterization, even when using high-resolution instruments. To overcome these drawbacks, we present here an effective microgradient chromatographic technique that yields specific fractions of enriched phosphopeptides compatible with LC-MS/MS analysis. The purpose of our study was to increase the number of identified phosphopeptides, and thus, the coverage of the sample phosphoproteome using the reproducible and straightforward fractionation method. This protocol includes a phosphopeptide enrichment step followed by the optimized microgradient fractionation of enriched phosphopeptides and final LC-MS/MS analysis of the obtained fractions. The simple fractionation system consists of a gas-tight microsyringe delivering the optimized gradient mobile phase to reversed-phase microcolumn. Our data indicate that combining the phosphopeptide enrichment with the microgradient separation is a promising technique for in-depth phosphoproteomic analysis due to moderate input material requirements and more than 3-fold enhanced protein identification.
Citace poskytuje Crossref.org
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