Influence of different proteomic protocols on degree of high-coverage identification of nonspecific lipid transfer protein 1 modified during malting
Jazyk angličtina Země Německo Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
19156768
DOI
10.1002/elps.200800530
Knihovny.cz E-zdroje
- MeSH
- chymotrypsin chemie MeSH
- hmotnostní spektrometrie MeSH
- ječmen (rod) MeSH
- jedlá semena chemie MeSH
- molekulární sekvence - údaje MeSH
- proteiny vázající mastné kyseliny MeSH
- proteomika metody MeSH
- rostlinné proteiny chemie MeSH
- sekvence aminokyselin MeSH
- transportní proteiny chemie MeSH
- trypsin chemie MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- chymotrypsin MeSH
- Ltp1 protein, barley MeSH Prohlížeč
- proteiny vázající mastné kyseliny MeSH
- rostlinné proteiny MeSH
- transportní proteiny MeSH
- trypsin MeSH
Both top-down (combining protein separation with MS analysis of intact proteins) and bottom-up (MS analysis of digested proteins) proteomic approaches were used for detailed characterization of nonspecific lipid transfer protein from barley malt. The aim was obtaining high-coverage of the primary structure of the proteins and the determination of PTMs such as lipid adduction and glycation. Here we present an influence of 15 proteomic protocols (differing in applied separation technique, enzyme and digestion procedure) on the extent of the coverage of the protein primary structure. The most successful protocols were in-gel digestion with trypsin of alkylated protein and in-solution digestions with trypsin or trypsin/chymotrypsin mixture of the nonalkylated protein. Totally, full sequence coverage based on the PMF and 85% sequence coverage based on the peptide fragmentation including PTMs was obtained.
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